Watkins SoyNilla, Vanilla Flavored Protein Powder with FiberAid. Net Wt. 7.7 oz. (220 g), Product #22090. Ingredients: Soy protein isolate (providing a minimum of 50 mg isoflavones per serving) & soy protein concentrate, fructose, maltodextrin, rice flour, FiberAid (Registered) (arabinogalactan), natural & artificial flavors, magnesium aspartate, soy fiber, dicalcium phosphate, soy lecithin, Chromium Chelavite (Registered). Recall # F-1821-2011

Lot # 3000280

Recalling Firm: Watkins Inc., Winona, MN, by e-mail on August 24, 2011, by letters on August 26, 2011, August 29, 2011 and August 31, 2011 and by press release on September 12, 2011. 

Manufacturers: Watkins Inc., Winona, MN;  

Century Foods International A Division of Hormel Foods Corp., Sparta, WI.

Firm initiated recall is ongoing.

SoyNilla contains undeclared Milk.

1,535 units

Nationwide and Canada

Fresh Hot Basil is also known as lemon or white basil. The product is sold in bulk at grocery stores without labeling or coding. There is no UPC on packages. Recall # F-1822-2011

No codes. No expiration dates.

Recalling Firm: M & H Produce, Seattle, WA, by telephone on September 1, 2011 and by fax on September 2, 2011.

Manufacturer: Sanith Ourn dba Asiana Harvest, Indiantown, FL. FDA initiated recall is ongoing.

Fresh Hot Basil is recalled due to the contamination of Salmonella.

80 lbs

WA

Semi-Soft Cheese, Mini Grayson style, 1 lb square blocks, wrapped in white paper, further packed into foil lined plastic bags. Recall # F-1823-2011

Unit: MG122-11

Meadow Creek Dairy, LLC, Galax, VA, by telephone and press release on August 22, 2011. FDA initiated recall is complete.

Product may be contaminated with Listeria monocytogenes.

12 lbs

VA

SunRidge Farms All Natural Milk Chocolate Covered Cranberries. Packaged in a) individual 6.5 oz packages, Item code: 086051, UPC 086700680513; and b) 10 lb bulk boxes, Item Code: 021315; UPC 086700213155. Recall # F-1824-2011

a) Lot code 0211176; b) lot code 3271003

Falcon Trading Co., Inc., Pajaro, CA, by press release and letters on September 12, 2011. Firm initiated recall is ongoing.

Firm received a complaint that a package of SunRidge Farms All Natural Milk Chocolate Cranberries actually contained Milk Chocolate Toffee Peanuts.

5,452 lbs

CA, ME MD, MT, NV, PA, AZ, MO, TX, CT, OR, LA

1) Soy Beginnings, Non-GMO Low-Fat Soy Flour, Net Wt . 40 lbs bags, Product Code for 40# 285100-NFB and Product Code for 1500# 285100-NFT, 1500 lbs totes, NEEDS TO BE FURTHER PROCESSED 2) NexSoy, Certified Non-GMO Low-Fat Soy Flour, Net Wt. 40 lb bags, NEEDS TO BE FURTHER PROCESSED. Recall # F-1825-2011

1) Lot numbers TF112210, TF102610, and TF102710 2) Lot numbers TF112210 and TF102610

Thumb Oilseed Producers' Cooperative, Ubly, MI, by letter on September 15, 2011. Firm initiated recall is ongoing.

The recall resulted from routine sampling programs conducted by the company which revealed salmonella bacteria in the finished product.

1092 (total for both brand names) 40 lb. bags and 42, 1500 lb. totes

IL, VT, MN, PA, NH, and Canada

Yankee Trader Seafood Lobster Spread 7 oz., 5 lb and 30 lb plastic containers. Recall # F-1826-2011

Lot numbers: Lot #0810lobsp and #0824lobsp Expiration Dates: 09/14/2011 and 09/28/2011

Yankee Trader Seafood, Ltd, Pembroke, MA, by telephone and follow-up letter on August 30, 2011. Massachusetts initiated recall is complete.

Undeclared allergens: Undeclared fish, egg and wheat.

6/30 lb; 4/5lb and 44/7 oz

RI, MA

"Dr. Clark Store" Turmeric Powder 1 Cup, Item # 10196-1; Product is a bright yellow granulated powder packaged in a clear flexible plastic ziplock-like bag. The product is a dietary supplement. Label on the product does not indicate intended use.; Product label reads in part: "Dr. Clark Store *** Potent & Pure without excipients *** Dietary Supplement *** Turmeric Powder *** 1 Cup *** Suggested Use: Persons 12 or more years of age take up to 1/4 tsp 3 times daily or as directed by a health professional. Expect yellow stool. *** Warning: If you are pregnant/lactating or have any history of liver, gall-bladder or gastrointestinal problems, please consult a Healthcare Professional prior to use. Recall # F-1827-2011

Lot Numbers: 10002, 10003, 10115

Self Health Resource Center, Chula Vista, CA, by e-mail and letters beginning on April 26, 2011 and May 4, 2011. Firm initiated recall is ongoing.

Products may contain elevated levels of lead.

115 units

Nationwide and Canada, Japan, Korea, United Kingdom

FJORD SUPERIOR Norwegian cure Smoked Salmon is produced using only Superior Quality Atlantic Salmon. In the True Norwegian Tradition, the salmon is hand cured and Naturally Smoked***NORWEGIAN CURE***FJORD SUPERIOR Norwegian Cure Smoked Salmon is sliced ready to use. Open the pack and serve at ambient room temperature on a toasted bagel with cream cheese, sliced onions and capers. ***HICKORY HOUSE***". SUPERIOR SMOKED SALMON SLICED RETAIL PACK 4 oz***Ingredients: HighLand farms Atlantic salmon***sugar, sodium nitrite (Preservative) natural hickory smoke***Keep frozen until used. Thaw under refrigeration immediately before use. Package cannot be re-packed in reduced oxygen packaging by the retail***701009 400258***24182***Net Wt 0.25 lb. Product of the USA". Recall # F-1832-2011

Batch 24182

Hickory Smokehouse Miami, Inc., Hialeah, FL, by telephone, fax, and e-mail beginning on August 10, 2011. Florida initiated recall is ongoing. 

Product samples collected and tested by Florida Department of Agriculture tested positive for Listeria monocytogenes.

25 cases

Netherlands

________________________________________

SeaPak Breaded Butterfly Shrimp, Family Size, Net wt. 22 oz (1 lb 6 oz) 623g, Ready-to-Fry breading & seasoning, UPC 100 41322 10254 6, Product Code 10302. The product is sold by the case and each case contains 8 - 22 oz. packages. Recall # F-1834-2011

Production date of concern is 7/25/2011 with Julian Date of 1003 1206 on the case, "Best By" Date of January 25, 2013

Recalling Firm: Rich Products Corp., Buffalo, NY, by press release on September 23, 2011.  

Manufacturer: Rich Products Corp., Brownsville, TX. Firm initiated recall is ongoing.

The product contains undeclared milk (whey) from the coating.

2,279 cases

Nationwide

Baltic Coast brand Herring Special Salted, 1.3kg - 2.86lb -1300g -- Product of Russia. The product is packaged in a round plastic container. Recall # F-1835-2011

Code number 20.02.11 PVI44AMIC2

Recalling Firm: TGF Production, LLC, Brooklyn, NY, by press release and letters dated June 16, 2011.

Manufacturer: Iriada International Ltd., St. Petersburg, Russia. New York initiated recall is complete.

The imported fish was found to be not properly eviscerated prior to processing based on sampling and analysis by New York State Department of Agriculture & Markets.

40 cases (4 x 1300 g containers per case)

NY, MA

Three Rivers brand Golden Raisins, Net wt. 400 gms. Recall # F-1888-2011

Product is uncoded.

Shata Trading, Inc., Brooklyn, NY, by press release on July 28, 2011 and letter dated July 28, 2011. New York initiated recall is complete.

The golden raisins were found to contain undeclared sulfites (816 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.

Unknown

NY State

 

1) Quick Foods All Natural BEEF KEBAB PITA with Pita Bread, Ground, Beef, Pepper, Salt, Sumac, Lettuce, Tomato, Onion sandwiches in 4 oz and 7 oz packages. Recall # F-1777-2011;

 

2) Quick Foods HONEY MUSTARD CHICKEN BREAST with Bun, 100% Chicken Breast, Provolone, Cheese, Honey Mustard sandwiches in 5.5 oz package. Recall # F-1778-2011;

 

3) Quick Foods Fresh Quality Since 1983 CLASSIC TURKEY SUB with bun, Turkey Breast, Swiss Cheese, Lettuce, Tomato sandwiches in 9 oz plastic packaging. Recall # F-1779- 2011;

 

4) Quick Foods CHICKEN QUESADILLA PITA sandwich with Pita, Chicken, Cheddar, Mozzarella, Taco Spices in 5.5 oz packaging. Recall # F-1780- 2011;

 

5) Quick Foods Fresh Quality Since 1983 CHEESEBURGER with Bun, Beef Patty, American Cheese sandwiches in 4.25 oz packaging. Recall # F-1781-2011;

 

6) Quick Foods Fresh Quality Since 1983 PHILLY BEEF STEAK with Bun, Beef, Provolone Cheese, Onion, Green Pepper, Pepper Seasoning sandwiches in 7 oz plastic packaging. Recall # F-1782-2011;

 

7) Quick Foods Fresh Quality Since 1983 PHILLY SUPER BEEF STEAK with Bun, Beef, Provolone Cheese, Onion, Green Pepper, Pepper Seasoning sandwiches in 9 oz plastic packaging. Recall # F-1783-2011;

 

8) Quick Foods New! Since 1983 BEEF & BIRD sandwiches with Bun, Roast Beef, Turkey, Swiss Cheese in 9 oz plastic packaging. Recall # F-1784-2011;

 

9) Quick Foods Fresh Quality Since 1983 SUPER HAM & CHEESE sandwiches with Sub Bun, Ham, American Cheese in 9 oz plastic packaging. Recall # F-1785-2011;

 

10) Quick Foods Fresh Quality Since 1983 TURKEY & SWISS ON CIABATTA BREAD sandwiches with Ciabatta Bread, Lettuce, Turkey, Swiss in 6 oz plastic packaging. Recall # F-1786-2011;

 

11) Quick Foods CORNED BEEF & SWISS sandwiches with Rye Bread, Corned Beef, Swiss Cheese, Dijon Mustard in 6.5 oz plastic packaging. Recall # F-1787-2011;  

 

12) Quick Foods CORNED BEEF & SWISS sandwiches with Rye Bread, Corned Beef, Swiss Cheese in 7 oz plastic packaging. Recall # F-1788-2011;

 

13) Quick Foods Fresh Quality Since 1983 BBQ BEEF sandwiches with Bun, Beef Patty, BBQ Sauce 6 oz plastic packaging. Recall # F-1789-2011;

 

14) Quick Foods DOUBLE CHEESEBURGER sandwiches with Bun, Beef Patty, American Cheese 7 oz plastic packaging. Recall # F-1790-2011;

 

15) Quick Foods Fresh Quality Since 1983 SKINLESS POLISH SAUSAGE SANDWICH $1.29 sandwiches with Bun, Polish Sausage, American Cheese 4.5 oz plastic packaging. Recall # F-1791-2011;

 

16) Quick Foods Fresh Quality Since 1983 TURKEY PITA sandwiches with Pita Bread, Turkey, Swiss Cheese 7 oz plastic packaging. Recall # F-1792-2011;

 

17) Quick Foods CHICKEN PARMESAN sandwiches with Pita, Chicken, Mozzarella, Pizza Sauce, Provolone Cheese 8 oz plastic packaging. Recall # F-1793-2011;

 

18) Quick Foods CHICKEN & CHEESE sandwiches with Bun, Chicken Patty, American Cheese 6 oz plastic packaging. Recall # F-1794-2011;

 

19) Quick Foods Fresh Quality Since 1983 HAM & CHEESE sandwiches with Sub Bun, Ham, American Cheese in 7 oz plastic package. Recall # F-1795-2011;

 

20) Quick Foods COMBO PITA sandwiches with Pita Bread, Ham, Bologna, Salami, American Cheese, Swiss Cheese in 8 oz plastic package. Recall # F-1796-2011;

21) Quick Foods Fresh Quality Since 1983 CLUB PITA sandwiches with Pita Bread, Ham, Turkey, American Cheese, Swiss Cheese in 6 oz plastic package. Recall # F-1797-2011;

 

22) Quick Foods Fresh Quality Since 1983 TURKEY & SWISS sandwiches with Sub Bun, Turkey, Swiss Cheese in 7 oz plastic package. Recall # F-1798-2011;

 

23) Quick Foods Fresh Quality Since 1983 SUPER ROAST BEEF sandwiches with Bun, Roast Beef, American cheese in 9 oz plastic package. Recall # F-1799-2011;

 

24) Quick Foods Fresh Quality Since 1983 SUPER TURKEY & CHEESE SUB sandwiches with Sub Bun, Turkey, Provolone Cheese in 9 oz plastic package. Recall # F-1800-2011;

 

25) Quick Foods Fresh Quality Since 1983 ITALIAN SUB sandwiches with Sub Bun, Ham, Hard Salami, Provolone Cheese, Pepper Rings, Lettuce, Tomato, Oregano in 7 oz plastic package. Recall # F-1801-2011;

 

26) Quick Foods Fresh Quality Since 1983 SUPER ITALIAN SUB sandwiches with Sub Bun, Ham, Hard Salami, Provolone Cheese, Pepper Rings, Lettuce, Tomato, Oregano in 9 oz plastic package. Recall # F-1802-2011;

 

27) Quick Foods Fresh Quality Since 1983 SUBMARINE sandwiches with Bun, Salami, Bologna, American Cheese, Ham, Pepper Rings in 7 oz plastic package. Recall # F-1803-2011;

 

28) Quick Foods CHICKEN SALAD sandwiches with Wheat Bread, Chicken, Mayonnaise, Celery, Hot Pepper Rings, Salt, Pepper in 6.5 oz plastic package. Recall # F-1804-2011;

 

29) Quick Foods Fresh Quality Since 1983 SUPER DELUXE TURKEY sandwiches with Bun, Turkey Breast, Hard Salami, Provolone Cheese, Lettuce, Tomato, Pepper Rings in 9 oz plastic package. Recall # F-1805-2011;

 

30) Quick Foods Fresh Quality Since 1983 GIANT SUBMARINE sandwiches with Bun, Salami, Bologna, Pepperoni, American Cheese, Ham, Pepper Rings in 10 oz plastic package. Recall # F-1806-2011;

 

31) Quick Foods Fresh Quality Since 1983 CLASSIC ITALIAN ON CIABATTA BREAD sandwiches with Ciabatta bread, Salami, Cappacuolo, Pepper Jack Cheese, Provolone Cheese, Pepper Rings in 7 oz plastic package. Recall # F-1807-2011

All codes produced 7/26/2011 - 08/10/2011.

Quick Food Co., Ferndale, MI, by visit on August 3, 2011. FDA initiated recall is ongoing.

Wheat is used as an ingredient and is not declared on the ingredient declaration. Yellow #5 is used in the pepper rings and is not identified as the ingredient declaration.

Unknown

MI

CBG 1000 (Peptide Bonded Glutamine Powder), Also known as Amino Peptide Blend. 

Recall # F-1819-2011

Lot # / Manufacture Date Lot 1004 CP = 10/2009 Lot 1005 CP = 04/2010 Lot 1006 CP = 10/2010 Lot 1007 CP = 02/2011

Commercial Proteins Corp., Lake Arrowhead, CA, by visit on September 19, 2011. FDA initiated recall is ongoing.

Commercial Proteins Corporation has confirmed CBG 1000 (Peptide Bonded Glutamine Powder) contains the allergen wheat and does not declare wheat on the product label.

3325 bags, 55lb/bag

CA, UT, WA, NJ, Poland and England

1) "Dr. Clark Purity Products" Turmeric Dietary Supplement, Item # 10349-100, 500mg, 100 Capsule bottle; Product is packaged in a white rigid plastic bottle. Label background is of a light gray color. The capsules are clear colorless gelatin capsules. When the Turmeric is encapsulated, the capsule appears yellow.; Product label reads in part: "Turmeric *** Dietary Supplement *** 500mg *** 100 capsules *** Directions: Adults take up to 2 capsules 3 times a day with meals, or as directed by a health professional. Children, 12 and over, take 1 capsule up to 3 times per day with meals, or as directed by a health professional. *** Expect yellow colored stool. *** Keep out of reach of children. *** Store at room temperature *** Supplement Facts *** Serving Size: 2 Capsules ***Serving per container: 50 *** Other ingredients: Easy to swallow gelatin capsules. Does not contain tablet binders, coatings or colorings. Recall # F-1828-2011;

 

2) "Dr. Clark Store Potent & Pure without excipients" Turmeric, Item #10349-100, 500mg, 100 Capsules bottle; Product is packaged in a white rigid plastic bottle. Label background is of a bright yellow color. The capsules are clear colorless gelatin capsules. When the Turmeric is encapsulated, the capsule appears yellow.; Product label reads in part: "Dr. Clark Store *** Potent & Pure without excipients *** Dietary Supplement *** Turmeric *** 500mg *** 100 Capsules *** Suggested use: Persons 12 yore more years of age, take up to 2 capsules 3 times daily or as directed by a health professional. Expect yellow stool. *** This is a whole, fresh, natural ground herb in its purest form. No extraction or chemical process applied. Helps to support a healthy inflammatory response. Warning: If you are pregnant/lactating or have any history of liver, gall bladder or gastrointestinal problems, please consult a Health Professional prior to use. Store this product dry and cool. Keep out of reach of children. Disclaimers: These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat a cure, or prevent any disease. Company doesn't adopt any Dr. Clark claims. Supplement Facts *** Serving Size: 2 Capsules *** Servings per container: 50. Recall # F-1829-2011;

 

3) "Dr. Clark Purity" Dr. Clark Quick ParaZap Cleanse, Item#50945-135, 520mg, 135 Capsule bottle; Product is packaged in a box. The capsules are clear colorless gelatin capsules. When the Turmeric is encapsulated, the capsule appears yellow. The product label declares 135 Capsules; Product label reads in part: "Dr. Clark Purity *** Dr. Clark *** Quick ParaZap *** Cleanse *** 2 *** 520mg *** 135 Capsules *** Dietary Supplement *** Dr. Clark Purity *** The Complete Colon Cleanse *** A Complete Colon Cleanse helps maintain optimum health in the entire digestive and urinary system, not only the colon. Complete all four cleanses in this order (1) Digestive Aid Helps maintain healthy pH in stomach (2) ParaZap Cleanse (3) Kidney Cleanse (4) Liver * Gallbladder Cleanse and FLUSH* *** Do not use if safety seal on bottle is broken. Keep out of reach of children. Store in a cool, dry place. Supplement Facts *** Serving Size: 14 Capsules *** Serving Per container: 9 *** Proprietary Blend 7,350mg *** Turmeric *** Black Walnut Hull *** Wormwood *** Anise Seed *** Cardamom Seed *** Coriander Seed *** Fennel Seed *** Cloves. Recall # F-1830-2011

1) Lot Numbers: 09005, 10006;

2) Lot Numbers: 09031, 10032, 10033;

3) Lot Numbers: 09006, 09007, 10008, 10009

Self Health Resource Center, Chula Vista, CA, by e-mail and letters beginning on April 26, 2011 and May 4, 2011. Firm initiated recall is ongoing.

Products may contain elevated levels of lead.

1) 5978 units; 2) 655 units; 3) 1663 units

Nationwide and Canada, Japan, Korea, United Kingdom

Quon Yick Chinese Dry Noodle, a) Regular and b) Medium sizes. Recall # F-1833-2011

No code information present.

Quon Yick Distributors, Inc., El Monte, CA, by letter on September 15, 2011. FDA initiated recall is ongoing.

Finished product packaging does not declare FD&C Yellow #5, FD&C Yellow #6, and FD&C Red #40. All three of these colors are ingredients contained in the noodle products.

a) 1503-30 lb boxes; b) 903-30 lb boxes

CO, NM, CA

Watkins Original Double Strength Vanilla, 2 Fl. oz. (59 mL), product #21390. Ingredients: Water, glucose, propylene glycol, vanilla extract (alcohol, water, extractive of vanilla beans), alcohol (8.25%), artificial flavors, caramel color. Recall # F-1820-2011

Lots: 3001497, 3002021, 3003887, 3005241

Recalling Firm: Watkins Inc., Winona, MN, by e-mail on August 24, 2011, by letters on August 26, 2011, August 29, 2011 and August 31, 2011 and by press release on September 12, 2011. 

Manufacturers: Watkins Inc., Winona, MN;  

Century Foods International A Division of Hormel Foods Corp., Sparta, WI.

Firm initiated recall is ongoing.

Double Strength Vanilla, 2 oz, is missing a declaration of sulfites.

1,535 units

Nationwide and Canada

"Dr. Clark Purity" Digestive Aid The Quick Colon-Bowel Cleanse, Item # 50951-125, 535mg, 125 capsule bottle; Product is packaged in a box consisting of paper material. The product label declares 125 Capsules. The capsules are clear colorless gelatin capsules. When the Turmeric is encapsulated, the capsule appears yellow.; Product label reads in part: "Dr. Clark Purity *** Quick *** Digestive Aid 1st Step in Colon Cleansing *** 1 *** For optimum results use with cleanse #2 Dr. Clark ParaZap *** 535mg *** 125 Capsules *** Dietary Supplement *** The Complete Colon Cleanse *** A Complete Colon Cleanse helps maintain optimum health in the entire digestive and urinary system, not only the colon. Complete all four cleanses in this order (1) Digestive Aid -Helps maintain healthy pH in stomach (2) ParaZap Cleanse (3) Kidney Cleanse (4) Liver * Gallbladder Cleanse and FLUSH* *** Supplement Facts *** Serving Size: 3 Capsules *** Serving Per container: 41 *** Proprietary Blend 1605mg *** Betaine HCL 945mg *** Papain *** Pepsin *** Turmeric *** Fennel Seed *** Other ingredients: Gelatin capsules. Does not container flow agents, tablet binders, coatings or colorings. *** Dr. Clark Purity *** Chula Vista, California 91911 *** Directions *** Always take with breakfast, lunch and dinner, or as directed by a health care professional. The first day take 1 capsule 3 times. From then on take 3 caps 3 times daily." Recall # F-1831-2011

Lot Numbers: 10001, 10226

Self Health Resource Center, Chula Vista, CA, by e-mail and letters beginning on April 26, 2011 and May 4, 2011. Firm initiated recall is ongoing.

Products may contain elevated levels of lead.

656 units

Nationwide and Canada, Japan, Korea, United Kingdom

 

 

 

No pending classifications this week.

 

RECALLS AND FIELD CORRECTIONS: DRUGS - CLASS I 

SLIM XTREME Herbal Slimming Capsule, 30 capsule bottles. Recall # D-1460-2011

All Lots

Recalling Firm: Globe All Wellness LLC, Hollywood, FL, by press release and email on May 24, 2011.

Manufacturer: Kunming Dali Industry & Trade Co, LTD, Shanghai, China. Firm initiated recall is ongoing.

Marketed Without an Approved NDA/ANDA: Product tested positive for Sibutramine, a appetite suppressant that was withdrawn from the U.S. market in October 2010 for safety reasons, making this product unapproved new drugs.

39,700 bottles

Nationwide and Internationally

1) X-Hero capsules with English label, 1 capsule pack, no UPC Code, 10 capsule bottles, UPC Code: 689087070995; X-Hero capsules with Chinese and/or English Label, 8 capsule bottles, UPC Code: 689076499255. Recall # D-1461-2011;

 

2) Male Enhancer capsules, 60 capsule bottles, UPC Code: 982010061205. Recall # D-1462-2011

All lots

Recalling Firm: U.S.A Far Ocean Group LLC, Alhambra, CA, by press release on March 28, 2011 and by letter beginning on April 14, 2011.  

Manufacturer: GuangZhou HeSheng Tang Daily Necessities Co., Ltd., Guangdong, China. Firm initiated recall is ongoing.

Marketed without an approved NDA/ANDA; FDA lab analysis found product to contain tadalafil, an FDA approved drug used to treat erectile dysfunction (ED), making the product an unapproved new drug.

111,918 capsules

Nationwide

Indomethacin for Injection USP, 1 mg, Single Dose Vials, Sterile, Rx only, For the Preparation of IV Solutions, NDC 55390-299-01. Recall # D-1578-2011

Lot #: 2271-01-1948138, Exp Date 09/11

Ben Venue Laboratories Inc., Bedford, OH, by letters on April 19, 2011. Firm initiated recall is ongoing.

Presence of Particulate Matter; 12 month stability.

11,902/1 mg vials

Nationwide

 

RECALLS AND FIELD CORRECTIONS: DRUGS - CLASS II 

1) First Aid Kits (plastic/metal/softpack) containing recalled Triad alcohol prep pads. Brands include North First Aid Kits, North Safety & Swift, and North by Honeywell. (The following are the Item #s and names on the kits: Item #s : 68200, GALLS REFILL 1ST RESPONDER, Exp. 01/11; 68203, GALLS FILL TRAUMA KIT, Exp. 01/11; 68222, S1111 ANAHEIM UNION LOGO/FAO 222-U, Exp. 01/11; 121054, CPR MICROSHIELD W/2 PR LTX GLV, Exp. 01/11; 121055, MICROSHLD W/LTX GLV /ALCL WIPE, Exp. 01/11; 145225, DELUXE TRAUMA KIT, Exp. 01/11; 148805, EMERGENCY MEDICAL FANNY PACK, Exp. 01/11; 148820, MAJOR TRAUMA KIT, Exp. 01/11; 148835, SURVIVAL PACK FANNY PACK, Exp. 01/11; 154818, ALCOHOL WIPES 50'S, Exp. 01/11; 155818, ALCOHOL PADS TRIAD 70% 100/BX, Exp. 01/11; 156818, ALCOHOL PADS MEDIUM 200/BX, Exp. 01/11; 346100, EMERG. MEDICAL KIT #1 SWIFT, Exp. 01/11; 346200, EMERG. MEDICAL KIT #2 SWIFT, Exp. 01/11; 662100, S0006 HEALER COMP 100 KIT 180 FAK, Exp. 01/11; 6805241, S0005 FA2000 TRUCK KIT FILL/FAK 460, Exp. 01/11; 6808139, S0003 IOWA IRR /FAK 10 UN STEEL, Exp. 01/11; 6810250, DIRECT SAFETY FILL/FAK 36UN ST, Exp. 01/11; 6814260, CITY OF DAYTON FILL/24U MTL FA, Exp. 01/11; 6816650, S0511 MCDONALD'S FILL / LOGO 24 UN, Exp. 01/11; 6842304, A M SUPPLY FILL/FAK 16UN PLSTC, Exp. 01/11; 6885416, AIRGAS REFILL FOR DUNN CONST; Exp. 01/11; 63157998, LSS CPR EMERGENCY KIT, Exp. 01/11; 63158006, LSS #24 ANSI FIRST AID KIT, Exp. 01/11; 64058008, 4646 RADNOR 25 PERSON FIRST AID KIT, Exp. 01/11; 64058013, RADNOR LOGO/420 KIT STEEL, Exp. 01/11; 64058014,RADNOR LOGO/24 UNIT STEEL KIT, Exp. 01/11; 64058022, 4649 RADNOR 16 UN PL TRUCK KIT, Exp.01/11; 64058023,4650 RADNOR 24 UN PL UNITIZED KIT,Exp.01/11; 64058025, 4661 RADNOR 16 UN STL KIT, Exp.01/11; 64058026, 4662 RADNOR 24 STL UNITIZED KIT, Exp. 01/11; 66019720, NORTH COMP 100 PERSON METAL, Exp.01/11; 010019-4320, 4320 24 UN ST KIT ENERGIES LG, Exp. 01/11; 010030-4434, 4434 24 UN PL ALAGASCO KIT, Exp. 01/11; 010057-3142, 3142 24 WH CITY OF ANAHEIM, Exp. 01/11; 010068-4509, 4509 16 WH CITY OF ANAHEIM, Exp. 01/11; 010153-3927, 3927 10 WH BN SANTA FE, Exp. 01/11; 010176-4247, 4247 24 UN METAL ALLIANT ENRGY, Exp. 01/11; 010177-4180, 4180 36 UN STL US AIRWAYS GRND, Exp.01/11; 010177-4248, 4248 36 UN METAL ALLIANT ENRGY, Exp. 01/11; 010183, 36U US AIRWAYS GROUND KIT, Exp. 01/11; 010192-3301, 3301 16 UN STL NASHVILLE ELECT, Exp. 01/11; 010310-2506, 2506 NORTH 10U WH CONTRACTOR, Exp. 01/11; 010310-4141, 4141 10 WH CNTRCTR W/NATIONAL, Exp. 01/11; 010316-2751, 2751 NORTH 16U WH CONTRACTOR, Exp. 01/11; 010316-4142, 4142 16 WH CNTRCTR W/NATIONAL, Exp. 01/11; 010321-2243, 2243 24 WH FISHER SCIENTIFIC, Exp. 01/11; 010324-2507, 2507 NORTH 24U WH CONTRACTOR., Exp. 01/11; 010324-4143, 4143 24 WH CNTRCTR W/NATIONAL, Exp. 01/11; 010336-2507, 2507 NORTH 36U WH CONTRACTOR, Exp. 01/11; 010336-4144, 4144 36 WH CNTRCTR W/NATIONAL, Exp. 01/11; 010370-4470, 4470 36 WH AIRGAS GASPRO, Exp. 01/11; 010385-3079, 3079/1724 10 PL NORTH/VALLEN, Exp.01/11; 010424-4224, 4224 36 UNIT METAL KIT W/PECO LOGO, Exp. 01/11; 010498-3502, 3502 16 WH HAWAIIAN ELECTRIC, Exp. 01/11; 010500-0475, 0475 16 WH HAWAIIAN DREDGING, Exp.01/11; 010552-3305, 3305 16 WH KC STHRN RR, Exp. 01/11; 010710-4078, 4078 24 WH CITY OF NAPERVILLE, Exp. 01/11; 010742-3236, 3236 16 WH N Y MOTOR POOL, Exp. 01/11; 010756-3126, 3126 16 WH NORTHERN ILLINO GAS, Exp.01/11; 010885-4514, 4514 24U CONOCO PHILLIPS, Exp. 01/11; 011011-4165N, 4165 24 WH SOUTHERN COMPANY, Exp. 01/11; 011084-4314, 4314 24 UN STL KIT ELVIN SAFET, Exp.01/11; 011122-3265, 3265 10 WH UCSD-UNIV CA-SN DGO, Exp. 01/11; 011501-4030, 6 WH CPR REGULAR SYSCO 4030, Exp. 01/11; 011542-4293, 4293 36 UN STL INTERNATI PAPER, Exp. 01/11; 011554-1724, DISASTER PREPAREDNESS KIT, Exp. 01/11; 011565-1725, 1725 16 UN STL IBT NORTH LOGO, Exp. 01/11; 011595-1724, 1724 16 PL NORTH SMART KIT, Exp. 01/11; 011598-4336, 4336 16 STL STUFFER COLUMBIA, Exp. 01/11; 011599-4338, 4338 10 UN BLOODBORNE COLUMBIA, Exp. 01/11; 011614-2527A, 2527A 24 UN STL MAGID NORTH, Exp. 01/11; 011623-4358, 4358 MED BULK STL COLUMBIA GAS, Exp. 01/11; 011642, 16U NORFOLK, Exp. 01/11; 011643, 36U NORFOLK, Exp. 01/11; 011670-1726, 1726 36 UN STL FISHER NORTH, Exp. 01/11; 012101-2636, 2636 MEDIUM BULK KIT AIR PROD, Exp.01/11; 012101-2959A, 2959A MEDIUM BULK KIT (#50), Exp. 01/11; 013005-4399, 4399 16U STL A&L UNDERGROUND, Exp. 01/11; 013010, REFILL KIT 013005-4399, Exp. 01/11; 013043-4433, 4433 10 UNIT PL SOUTH DAKOTA, Exp. 01/11; 013061-4454, 4454 24 UNIT STL CEE US, Exp. 01/11; 013087-1725A, 1725A 16 UN 16 STL, Exp. 01/11; 013091-4543, 4543 16U STL VIKING LOGGERS, Exp. 01/11; 013094-4506, 4506 10P PL ABATIX ANSI BULK, Exp. 01/11; 013101-0005L, 0005L 10U STL ATMOS ENERGY W/NORTH, Exp. 01/11; 013103-0008L, 36 UN STL GRAINGER/NORTH KIT, Exp. 01/11; 013104-0008L, 36U PL GRAINGER/NORTH KIT, Exp. 01/11; 013108-4534, 4534 150P CAB MEDSAFE F/A, Exp. 01/11; 013109-4535, 4535 200P DXL CAB MEDSAFE F/A, Exp. 01/11; 013113-4545, 4545 25 PERSON STL FA MEDSAFE, Exp.01/11; 013113-4612, 4612 25 PERSON STL UNIVERSAL LOGO, Exp. 01/11; 013115, 150P REFILL KIT MEDSAFE, Exp. 01/11; 013116, 200P REFILL KIT MEDSAFE, Exp. 01/11; 013134-4374, 4374 10 UN STL PROGRESS ENERGY, Exp. 01/11; 013142-4483, 4483 24 UNIT STL VIKING, Exp. 01/11; 013142-4483, 4483 24 UNIT STL VIKING, Exp. 01/11; 013147-4596, 4596 10 UN STL AIRGAS/ FIRST AID, Exp.01/11; 013161-0008L, 0008L 36 UNIT BPXA KIT W/NORTH LOGO, Exp. 01/11; 014050-4214, SPORTSMAN KIT W/NORTH, Exp. 01/11; 014100-4212, HOME/OFFICE KIT W/NORTH, Exp. 01/11; 015310-3839, 3839 6 WH CPR COM ED LOGO, Exp.01/11; 015451-2596, 2596 16 WH HUNTSVILLE UTILITIE, Exp. 01/11; 016000-0000, 6 DISPOSABLE CPR KIT, Exp. 01/11; 018511-4222, COLUMBIA SOFT PACK W/NORTH, Exp.01/11; 018512-4219, 4219 SOFT PACK PROMOTIONAL RETAIL, Exp/ 01/11; 019000-2396A, 2396A LG FIRST AID CABINET, Exp. 01/11; 019000-4264, 4264 LG CABINET W/VWR INT'L, Exp. 01/11; 019001-0000, DELUXE FIRST AID CABINET 2395, Exp. 01/11; 019001-2395A, 2395A DELUXE FIRST AID CABINET, Exp. 01/11; 019001-4262, 4262 DXL CABINET W/VWR INT'L, Exp. 01/11; 019023, REFILL LG CAB, Exp. 01/11; 019089-3462A , 3462A MED FIRST AID CABINET, Exp. 01/11; 019089-4026, 4026 FIRST AID CABINET SYSCO, Exp.01/11; 019089-4266, 4266 MED FA CABINET VWR INT'L, Exp.01/11; 019642-4366, 4366 16 PL NORFOLK, Exp.01/11; 019643-4367, 4367 36 UN PL NORFOLK, Exp. 01/11; 019651-4375, 4375 24 UN STL AIRGAS/ LUCENT, Exp. 01/11; 019720, REFILL 100P FA STATION NORTH, Exp.01/11; 019720-0009L, 100P CABINET NORTH, Exp. 01/11; 019720-0009L/L, 100P CABINET NORTH LAB, Exp. 01/11; 019720-4489, 4489 100P CABINET VIKING ANSI, Exp. 01/11; 019720-4516, 100P CABINET NORTH, FISHER, Exp. 01/11; 68400LCP, S0681 COLE-PARMER LOGO 400/LN STAN, Exp. 01/11; 68400LEG, S0684 EVERGREEN LOGO/STD FILL W/LINR, Exp. 01/11; 68400LELV, S0006 ELVIN FILL 400L SUPERVAL BLANK, Exp. 01/11; 68400LELVRF, ELVIN FILL 400L SUPERVAL REFIL, Exp. 01/11; 68400LFAPS, S0674 APS FILL/LOGO 400 KIT W/LINER, Exp. 01/11; 68400LFLP, S0006 LAWSON FILL 4 SHELF FAK LOGO, Exp.01/11; 68400LGETZ, GETZ LOGO 4 SHELF STAN W/LINER, Exp. 01/11; 68400LISP, S0699 ISP LOGO/FILL W/LINER 4 SHELF, Exp. 01/11; 68400LISS, S0700 IND.SAFETY LOGO/STD FILL W/LNR, Exp. 01/11; 68400LMAX, SAFETY MAX LOGO/400 STAN-LINER, Exp. 01/11; 68400LMM, S0720 MOBIL MED LOGO 400 STAN LINER, Exp. 01/11; 68400LNODEA, S0006 STANDARD 4 SHELF NO COLD TABS, Exp. 01/11; 68400LNT, S0006 400 KIT WITHOUT TABS W/LINER, Exp. 01/11; 68400LQC, S075 QUAD CITY FILL/LOGO 400 W/LNER, Exp. 01/11; 68400LST, SAFETY 2 DAY LOGO 400L STAN, Exp.01/11; 68400LWAOX, S0723 OXARC-WASH FILL/LOGO 400 LINER, Exp. 01/11; 68400LWS, WILLIAMS SONOMA FILL/FAK 400WL, Exp.01/11; 68400PD, PAYNE & DOLAN SPC/ 4 SH FAK, Exp.01/11; 68400RFNODEA, 1EF.FOR 68-400NODEA NO COLD TB, Exp. 01/11; 68401LRFS, RELIABLE FIRE LOGO/STD 401 KIT, Exp. 01/11; 68401LWAYEST, S0734 WAYEST SAFETY LOGO/STD 401 W/L, Exp. 01/11; 68499AB, ABATIX FILL FAK LOGO SPECIAL, Exp. 01/11; 68600MJ, S0866 MJ HARRIS LOGO 5 SHELF IND FIL, Exp. 01/11; 68600NODEA, 600 XL INDUS./FAK NO COLD TABS, Exp. 01/11; 68600PROAM, S0006 PROAM SPEC FILL 5 SHELF IND FA, Exp. 01/11; 68601FA2, FA2000 LRG IND LOGO + CPR, Exp. 01/11; 6888EFA, EMERGENCY FIRST AID RESPONDER, Exp. 01/11; 682100HERS, HERTZ LOGO/FILL 100 PER, Exp. 01/11; 68300AM, S0371 A & M LOGO/STD FILL W/LINER, Exp. 01/11; 6834180LF, 4883 RITZ LOGO 3 SHELF INDUST W LIN, Exp. 01/11; 6834400LF, 4884 RITZ SAFETY 4 SHELF IND W/LIN, Exp. 01/11; 6834600F, 4885 RITZ LOGO 5 SHELF INDUSTRIAL, Exp. 01/11; 6836TT, TOTAL TOOL SPEC FILL FAK, Exp. 01/11; 68400AM, S0673 A & M LOGO/STD FILL W/LINER, Exp. 01/11; 68400HMYR, HAGEMEYER/ SPC 4 SHELF FAK, Exp. 01/11; 68400LABC, S0671 ABC FIRE LOGO/STD FILL W/LINER, Exp. 01/11; 68400LBB, S0676 BENNETT BOWEN LOGO/400 NO DEA, Exp. 01/11; 64058000, 4641 RADNOR HEAVY INDUSTRIAL STATS, Exp. 01/11; 64058000RF, RADNOR REFILL FOR 5 SHELF, Exp. 01/11; 64058001, 4640 RADNOR HEAVY INDUSTRIAL STATS, Exp. 01/11; 64058001RF, RADNOR REFILL FOR 4 SHELF, Exp. 01/11; 64058004, 4638 RADNOR HEAVY INDUSTRIAL STATS, Exp. 01/11; 64058004RF, RADNOR REFILL FOR 3 SHELF, Exp. 01/11; 6810300, 4847 FA2 LOGO 180 STAN WITH LINER, Exp. 01/11; 6810300FTC, 4847 FORT COLLINS FILL/FA2 LOGO 180, Exp. 01/11; 6810444FTC, 4856 FORT COLLINS FILL/FA2 LOGO 400, Exp. 01/11; 6810662, MCDONALD'S REFILL # 010662, Exp. 01/11; 019720-4516F, 100P CABINET NORTH, FISHER, Exp. 01/11; 019720-4586, 4586 100P CABINET SAFE SITE SUPPLY, Exp. 01/11; 019721, REFILL 150P FA STATION NORTH, Exp. 01/11; 019721-0010L, 150P CABINET NORTH, Exp. 01/11; 019721-4490, 4490 150P VIKING STATION ANSI, Exp. 01/11; 019721-4517F, 150P CABINET NORTH, FISHER, Exp. 01/11; 019721-4586, 4586 150P SAFE SITE SUPPLY, Exp. 01/11; 019722, REFILL 200P FA STATION NORTH, Exp. 01/11; 019722-0011L, 200P CABINET NORTH, Exp. 01/11; 019722-4491, 4491 200P CABINET VIKING ANSI, Exp. 01/11; 019722-4518F, 200P CABINET NORTH, FISHER, Exp. 01/11; 019729-0016L, 10U STL NORTH CONSTRUCTION KIT, Exp. 01/11; 019729-4492, 4492 10U STL VIKING CONSTRUCTION, Exp.01/11; 019730-0017L, 16U STL NORTH CONSTRUCTION KIT, Exp. 01/11; 019730-4493, 4493 16U STL VIKING CONSTRUCTION, Exp. 01/11; 019731-0018L, 24U STL NORTH CONSTRUCTION KIT, Exp. 01/11; 019731-4494, 4494 24U STL VIKING ANSI, Exp. 01/11; 019731-4521, 24U STL NORTH CONSTRUCTION KIT, FISH, Exp. 01/11; 019732-0019L, 36U STL NORTH CONSTRUCTION KIT, Exp. 01/11; 019732-4495, 4495 36U STL VIKING CONSTRUCTION, Exp. 01/11; 019735-0022L, 6U STL NORTH CPR KIT, Exp. 01/11; 019741-0028L, NORTH BITE & STING KIT, Exp. 01/11; 019741-0028L/LA, NORTH BITE & STING KIT, Exp. 01/11; 019751-0020L, 0020L HIP POCKET KIT NORTH, Exp. 01/11; 019751-4393, 4393 HIP POCKET KIT PL VWR, Exp. 01/11; 019751-4501, 4501 COMPACT STAUFFER KIT, Exp. 01/11; 021047, ALCOHOL PREP PADS 10P, Exp. 01/11; 032525, O/H PAK ALCOHOL WIPES 100 PER, Exp. 01/11; 148820RF, MAJOR TRAUMA KIT REFILL, Exp. 01/11; 340410F, TRK KIT STEEL WP FAK LOGO SM, Exp. 01/11; 340410FP, TRK KIT STL WP FAK LOGO W/PUMP, Exp. 01/11; 340460F, TRUCK KIT DELUXE FAK LOGO, Exp. 01/11; 340460FP, S0005 TRUCK KIT DELUXE WP FAK W/PUMP, Exp. 01/11; 34410RF, TRUCK KIT STEEL WP REFILL, Exp. 01/11; 34460RF, REFILL FOR 34-0460 TRUCK KIT, Exp. 01/11; 346200RF, EMERG. MEDICAL KIT 2 REFILL, Exp. 01/11; 34T200, TRAUMA KIT IN DIVIDER BAG, Exp. 01/11; 34TRAM1, FIRST AID KIT TRAUMA #1, Exp. 01/11; 35224AS, ALCOHOL WIPES MEDIUM 100'S, Exp. 01/11; 3524CA, 24 UN STL CONTRACTOR KIT ANSI FAK, Exp. 01/11; 3524CF, 24 UN CONTRACTOR KIT FAK LOGO, Exp. 01/11; 3536CF, 36 UN STL CONTRACTOR KIT FAK LOGO, Exp. 01/11; 35P24CA, S0004 24 UN CONTRACTOR ANSI FAK 24 U, Exp. 01/11; 63111KTSRF, JUMP KIT REFILL, Exp. 01/11; 64058008RF, RADNOR REFILL FOR 25 PERSON KT, Exp. 01/11; 64058013RF, RADNOR LOGO/420 KIT STEEL, Exp.01/11; 64058013V, RADNOR LOGO/16 UNIT STEEL VERT, Exp. 01/11; 64058014RF, RADNOR LOGO/24 UNIT REFILL, Exp. 01/11; 6425RADSPEC, S0578 RADNOR LOGO/FILL #25 (DELTA), Exp. 01/11; 662010G, S0003 HEALER COMP 10 PER STEEL W/GSK, Exp/ 01/11; 662010P, S0003 HEALER COMP 10 PER PLAST W/GSK, Exp. 01/11; 662025P, S0004 HEALER COMP 25 PERSON PLASTIC, Exp. 01/11; 662050P, HEALER COMP 50 PERSON PLASTIC, Exp. 01/11; 66223ANB, FAO 223-AN #25 BULK ANSI/BARR, Exp. 01/11; 663024U, HEALER COMP 24 UNIT STEEL FAK, Exp. 01/11; 66B3304PE, FIRST RESPONDER TRAUMA KIT LG, Exp. 01/11; 66TK023, DYNA MED QUICK RESPONSE REFILL, Exp.01/11; 66TK029, DYNA MED BLS TRAUMA KIT REFILL, Exp.01/11; 67CHPKCPR, CPR KIT FOR SF00001424, Exp. 01/11; 680410MB, MANHATTAN BEACH FILL/FAK 410F, Exp. 01/11; 680460BKF, NO LOGO TRUCK KIT DELUXE,Exp. 01/11; 68058008E, S0931 RADNOR LOGO/25P FILL W/WOVEN, Exp. 01/11; 68058008ERF, REFILL KIT FOR 68058008E, Exp. 01/11; 6810BR, S0131 BELFOR LOGO/HEALER 2010G FILL, Exp. 01/11; 6810MD, S0172 MCDONALD SAFETY 10U STEEL LOGO, Exp. 01/11; 6810PE, S0178 CPR EMERGENCY KIT 10 U STL, Exp. 01/11; 6810PLOGAN, S0182 LOGAN GEN 10 PER PLAST W/GSK, Exp. 01/11; 6810PMD, S0183 MCDONALD SA 10 PER PLAST W/GSK, Exp. 01/11; 6810RH, ROBERT HEELY FILL/DSS LOGO 10U, Exp. 01/11; 6810RSAUTO, S0190 RIVERSIDE LOGO AUTO/ADMIN 10, Exp. 01/11; 6810VAIR, AIRGAS SPEC FILL VEH 10 KIT, Exp. 01/11; 6810WD#2 , S0199 WELDMARK LOGO / FILL 10 UN #2, Exp.01/11; 68120QCS, S0004 QUAD CITY FILL/FAK LOGO 120, Exp. 01/11; 68120RJS, S0004 RJ SAFETY FILL/FAK 120 KIT, Exp. 01/11; 68120RJSRF, RJ SAFETY REFILL FOR 120 KIT, Exp. 01/11; 681212ETJ EMS, TRAUMA JUMP KIT 12X12X10, Exp. 01/11; 68140PANDA, SW002 PANDA EXPRESS FILL/LOGO 140, Exp. 01/11; 68140PANDARF, REFILL FOR 68140PANDA, Exp. 01/11; 68140PROAM, PROAM SPEC FILL 2 SHELF IND FA, Exp. 01/11; 6816PROGE, SW031 PROGRESS ENERGY 16 U STL KIT, Exp. 01/11; 6816SM, S0364 STATE OF MICHIGAN LOGO/FILL 16, Exp. 01/11; 6816WD#2 , WELDMARK LOGO / FILL 16 UN #2, Exp. 01/11; 6816WRIGHT, SW005 WRIGHT BRO LOGO/FILL 16U STEEL, Exp. 01/11; 68180ARB, ARBILL FILL/FIRST AID STATION, Exp. 01/11; 68180LELVB, ELVIN SAFETY BAKERY 180L BLANK, Exp. 01/11; 68180LELVBRF, ELVIN SAFETY BAKERY 180L REFIL, Exp. 01/11; 68180LELVM, ELVIN MEAT DEPT FILL 180L BLK, Exp. 01/11; 68180LELVMRF, ELVIN MEAT DEPT FILL 180 REFIL, Exp. 01/11; 68180LELVRF, ELVIN SAFETY FILL 180L REFILL, Exp. 01/11; 68180NSC 4935, NORTHERN SAFETY #100 BULK KIT, Exp. 01/11; 682010GSSI, S0195 SSI LOGO /FILL 2010G COMP 10 S, Exp. 01/11; 682010PISP, INDUST SAFETY P10 FILL LOGO, Exp. 01/11; 68201TEX, S1076 TEX LOGO/FILL 24 UNIT PLASTIC, Exp. 01/11; 682025PSSI, SSI LOGO /FILL 2025P COMP 25 P, Exp. 01/11; 682025SSI, SSI LOGO /FILL 2025 COMP 25 ST, Exp. 01/11; 682050SSI, SSI LOGO /FILL 2050 COMP 50 ST, Exp. 01/11; 6824ALTEC, S0468 ALTEC FILL/LOG 2 MAN KIT STEEL, Exp. 01/11; 6824CSS#2, S0004 C&S SAFETY FILL/24UN FAK LOGO, Exp. 01/11; 6824FS, S0490 24U STL FILL W/CAL FIRE LOGO, Exp. 01/11; 6824LG, S0504 LACLEDE GAS FILL/LOGO 24U STL, Exp. 01/11; 6824NEI, NEW ELECTRIC FILL/ 24U MT FAK, Exp. 01/11; 6824PROGE, SW032 PROGRESS ENERGY 24 U STL KIT, Exp. 01/11; 6824PROGERF, PROGRESS ENERGY 24 U REFILL, Exp. 01/11; 6824PS, PUGET SAFETY LOGO/24 UNIT FILL, Exp. 01/11; 6824WAY, WAYEST SPEC FILL 24 UNIT FAK, Exp. 01/11; 6824WS, S0004 WINDSTREAM/FAK LOGO 24 UNIT, Exp. 01/11; 6825REC, S0579 RECREONICS FILL/LOGO 25 MAN, Exp. 01/11; 6825SH, S0584 SHARPE SAFETY #25 FILL/LOGO, Exp. 01/11; 6825TT, S0588 TOTAL TOOL FILL/LOGO 25 PER, Exp.01/11; 683024HERS, S0492 HERTZ LOGO/FILL 24U STL, Exp. 01/11; 683036HERS, HERTZ LOGO/FILL 36U STL, Exp. 01/11; 6836ALPD3, S0005 AIRGAS "PAYNE" 36U FILL/FAK #3, Exp. 01/11; 6836CHOC, CHOCTAW KAUL FILL/ 36U ST FAK, Exp. 01/11; 6836JEA, S0638 JACKSONVILLE ELEC FILL & LOGO, Exp. 01/11; 6836JEDUNN, S0639 JEDUNN LOGO/ SPC 36U METAL, Exp. 01/11; 6836M, S0005 MEMCO FILL/FAK 36 UNIT KIT, Exp. 01/11; 68400ARTIC, ARTIC FIRE CUSTOM 4 SHELF IND, Exp. 01/11; 68410GASESP, S0736 GASES PLUS LOGO/410 TRUCK KIT, Exp. 01/11; 68410GETZ, GETZ LOGO 410 STAN FILL (SML), Exp. 01/11; 68420FA22 , S0751 FA2000#2 FILL/LOGO MED TRK KIT, Exp. 01/11; 68460APS, APS LOGO TRUCK KIT DELUXE, Exp. 01/11; 68460GASESP, S0633 GASES PLUS LOGO/460 TRUCK KIT, Exp. 01/11; 68460GETZ, GETZ LOGO 460 STAN FILL (LRG), Exp. 01/11; 68460MM, S0645 MOBIL MED LOGO 460 STAN, Exp. 01/11; 68460SM, S0776 SAFETY MAX LOGO STAN FILL 460, Exp. 01/11; 68460ST, SAFETY 2 DAY LOGO 460 STAN, Exp. 01/11; 68EDRF, KINKOS REFILL KIT FOR 68180ED, Exp. 01/11; 68LAUSDKIT, LAUSD EMERGENCY FIRST AID KIT, Exp. 01/11; 68LAUSDRF, LAUSD REFILL KIT, Exp. 01/11; 68LFFLRF, REFILL FOR #68180LFFL, Exp. 01/11; 68P24AIR, SAIC FILL/LOGO 24 PLAS, Exp. 01/11; 68PRLRF, RE-FILL FOR 68PRLF, Exp. 01/11; 68SOFTPACK, NORTHERN SAFETY SOFTPACK, Exp. 01/11; 69099SC, L. A. UNIF SCH 164751-2, Exp. 01/11; 68180LBR, SW050 BRONER LOGO/STD 180 KIT W/LINR, Exp. 01/11; 68180LDSS, DIRECT SAFETY LOGO/STD 180 W/L, Exp. 01/11; 68180LDUNN, JE DUNN LOGO 3 SHELF HEAVY IND, Exp. 01/11; 68180LEG, EVERGREEN LOGO 180 STAN LINER, Exp. 01/11; 68180LFAPS, S0372 APS FILL/LOGO 180 KIT W/LINER, Exp. 01/11; 68180LFAST, S0392 FASTENAL LOGO 180 STAN W/LINER, Exp. 01/11; 68180LFASTSPEC, FASTENAL LOGO 180 SPEC W/LINER, Exp. 01/11; 68180LFCNS, S0006 NATIONAL SAFETY FILL/FAK 180, Exp. 01/11; 68180LFFL , KROGER FILL/FOOD4LESS LOGO W/L, Exp. 01/11; 68180LGETZ, GETZ LOGO 3 SHELF STAN W/LINER, Exp. 01/11; 68180LISPFA, ISP FILL W/LINER 3 SHELF FAK, Exp. 01/11; 68180LISS, S0404 IND.SAFETY LOGO/STD FILL W/LNR, Exp. 01/11; 68180LK, S0405 KROGER FILL/LOGO 3 SHF W/LINER, Exp. 01/11; 68180LMAX, S0421 SAFETY MAX LOGO/STAN 180-LINER, Exp. 01/11; 68180LMM, S0422 MOBIL MED LOGO 180 STAN LINER, Exp. 01/11; 68180LQC, S0430 QUAD CITY FILL/LOGO 180 W/LNER, Exp. 01/11; 68180LR, S0431 KROGER FILL/RALPH'S LOGO W/LNR, Exp. 01/11; 68180LRFS, RELIABLE FIRE LOGO/STD 180 KIT, Exp. 01/11; 68180LRS, RELIABLE SAFETY LOGO/FILL 180, Exp. 01/11; 68180LS, S0437 KROGER FILL/SMITH'S LOGO W/LNR, Exp. 01/11; 68180LST, S0440 SAFETY 2 DAY LOGO 180L STAN, Exp. 01/11; 68180LTJ, S0442 TRADER JOES FILL & LOGO 180W/L, Exp. 01/11; 68180LWAOX, S0427 OXARC-WASH FILL/LOGO 180 LINER, Exp. 01/11; 68180LWAYEST, S0444 WAYEST SAFETY LOGO/STD 180 W/L, Exp. 01/11; 68180LWHITES, S0447 WHITE SPUNNER LOGO 180 3 SHELF, Exp. 01/11; 68180OCE, SW106 OIL CAPITOL EL LOGO/STD 3 SHLF, Exp. 01/11; 68180SHAW, S0006 SHAW FILL/ 3 SHELF FAK, Exp. 01/11; 68140PRL, PRL FILL/ SPC 2 SHELF FAK, Exp. 01/11; 681800LNT, 3 SHELF IND NO TABS FAK LOGO, Exp. 01/11; 68180ED, S0006 KINKOS FILL/FAK LOGO 3 SHELF, Exp. 01/11; 68180ELVIN, S0387 ELVIN SAFETY LOGO 180 FILL, Exp. 01/11; 68180ENCHANT, S0388 ENCHANTMENT LOGO/STAN 180 FILL, Exp. 01/11; 68180FEDX, S0006 FED X FILL FAK LOGO 180 KIT, Exp. 01/11; 68180FOOD, S0419 OXARC FOOD SERVICE 3 SHELF, Exp. 01/11; 68180FRYS, S0396 FRYS LOGO/3 SHELF KIT, Exp. 01/11; 68180GUCKRF, GUCKENHEIMER SPEC 180 REFILL, Exp. 01/11; 68180LABC, S0369 ABC FIRE LOGO/STD FILL W/LINER, Exp. 01/11; 68120ARB, ARBILL FILL/FAK OFFICE KIT 120, Exp. 01/11; 68140BO, S0242 BOJANGLES FILL & LOGO 140 KIT, Exp. 01/11; 68140BUFF, BUFFET FILL/FAK 2 SHELF KIT, Exp. 01/11; 68140DATA, OCHARLEY'S FILL/DATA-SOURCE KI, Exp. 01/11; 68140FEDX, S0006 FED X FILL FAK LOGO 140 KIT, Exp. 01/11; 68140FLBK, S0267 BURGER KING FILL/LOGO 2 SHELF, Exp. 01/11; 68140FLBKRF, BURGER KING REFILL KIT, Exp. 01/11; 68140FOOD, S0298 OXARC FOOD SERVICE 2 SHELF, Exp. 01/11; 68140LFAPS, APS FILL/LOGO 140 KIT W/LINER, Exp. 01/11; 68140LJEDUNN, S0276 JEDUNN FILL (MEMCO)2 SHLF LOGO, Exp. 01/11; 68499FA22 , FA2000 FILL 499 HANDY KIT FAK, Exp. 01/11; 6850SH, S0660 SHARPE SAFETY #50 FILL/LOGO, Exp. 01/11; 685741A, SHELF RELIANCE KIT "A" ZIP BAG, Exp. 01/11; 685741B, SHELF RELIANCE KIT "B" ZIP BAG, Exp. 01/11; 685741BB, S0821 SHELF RELIANCE KIT "B" LOGO, Exp. 01/11; 685741C, SHELF RELIANCE KIT "C" ZIP BAG, Exp. 01/11; 68600ARTIC, ARTIC FIRE CUSTOM 5 SHELF IND, Exp. 01/11; 686100LONE, LONESTAR SAFETY FILL 6100 BAG, Exp. 01/11; 688805PA, PROAM FILL/EMER.MED.LOGO FANNY, Exp. 01/11; 688820FW, FRED WEBER FILL MAJOR TRAUMA K, Exp. 01/11; 688820IBT, IBT TRAUMA FILL, Exp. 01/11; 6888GATEWAy, GATEWAY FILL / SOFT BAG EM MED, Exp. 01/11; 68AG70, S0005 MJ ELECT FILL/FAK W/MJE DECAL, Exp. 01/11; 68AGT, AIRGAS TRAUMA KIT SPEC. REFILL, Exp. 01/11; 68B3303PRO, PROGRESS ENERGY SPEC FILL RED, Exp. 01/11; 68FA4, MY-BAGS.COM REFILL FA-4, Exp. 01/11; 68FERNOBLS#2, FERNO BLS PLASTIC BAG 12/C #2, Exp. 01/11; 68GS10, NO LOGO RANBERRY FILL 10UN STL, Exp. 01/11; 68GS16, GRANBERRY FILL/BLANK 16UN STL, Exp. 01/11; 68GS36, GRANBERRY FILL/BLANK 36UN TRUK, Exp. 01/11; 68MEDBAG, AIRGAS SPEC FILL MED PLAIN BAG, Exp. 01/11; 68MOD3, LIFESECURE QUICK RESP MOD 3, Exp. 01/11; 68P05241, S0005 FA2000 TRUCK KIT/FAK PLST 460, Exp. 01/11; 68P10ARB, S0003 ARBILL FILL/BULK FIRST AID KIT, Exp. 01/11; 68P10BBL, BENNETT-BOWEN FILL FAK 24 PLAS, Exp. 01/11; 68P10BR, SW047 BRONER LOGO/FILL #10 PLASTIC, Exp. 01/11; 68P10SAFKP, S0003 SAFETYKITSPLUS FILL/16 UNIT PL, Exp. 01/11; 68P10SCHW, S0003 SCHWARZ FILL PLAS BULK FAK, Exp. 01/11; 68P10SF, S0065 FORESTRY LOGO 10U FILL PLASTIC, Exp.01/11; 68P10WEGMANS, WEGMANS FILL/LOGO 10U PLASTIC,Exp. 01/11; 68P16HM#3, S1022 HENKELS-MCCOY FILL & LOGO 16UP, Exp. 01/11; 68P16TREN, S0004 TRENCH-IT FILL 16U PLAST FAK, Exp. 01/11; 68P2010, 10 PERSON PLASTIC FAK LOGO 10P, Exp. 01/11; 68P2025P, 25 PERSON PLASTIC FAK LOGO 16P, Exp. 01/11; 68P24COT, CITY OF TACOMA/ FAK 25 PERSON, Exp. 01/11; 68P24TE, S0004 TEXAS ELECTRIC FILL/FAK 24U PL, Exp. 01/11; 68P25ED, S1082 EQUIP DIR FILL/LOGO 25 PERSON, Exp. 01/11; 68P36DOTFL, FLORIDA DOT FILL/LOGO 36U PLAS, Exp. 01/11; 68P36MCM S1098, MCM CONSTRUCTION FILL PLA LOGO, Exp. 01/11; 68STING, STING KIT IN A ZIP LOCK BAG, Exp. 01/11; 68T200AM, HART SPECIAL FILL T200 KIT, Exp. 01/11; 68T24PROE, SW032 PROGRESS ENERGY TRUCK KIT LOGO, Exp. 01/11; 68T24PROE SW032 PROGRESS ENERGY TRUCK KIT LOGO, Exp. 01/11; 68TK046PSC, DYNAMED DELUXE TRAUMA/02 REFIL, Exp. 01/11; 68VDRA, VOLUNTEER DISASTER RESP. KIT A, Exp. 01/11; 68VDRR, VOLUNTEER DISASTER REPL.ITEMS, Exp. 01/11; 68XS10BT, 10 PERSON FAK IN PLASTIC BOX, Exp. 01/11; 130001CL, BASIC IRK W/54501CBRN, LARGE, Exp. 01/11; 130001CL/LAB, BASIC IRK W/54401CBRN, LARGE, Exp. 01/11; 130001CM, BASIC IRK W/54501CBRN, MEDIUM, Exp. 01/11; 130001CM/LAB, BASIC IRK W/54401CBRN, MEDIUM, Exp. 01/11; 130001CS, BASIC IRK W/54501SCBRN, SMALL, Exp. 01/11; 130001HL, BASIC IRK W/ER2000CBRN, LARGE, Exp. 01/11; 130001HM, BASIC IRK W/ER2000CBRN, MEDIUM, Exp.01/11; 130001HS, BASIC IRK W/ER2000CBRN, SMALL, Exp. 01/11; 130001L, BASIC IRK, LARGE, Exp. 01/11; 130001L/LAB, BASIC IRK, LARGE, Exp. 01/11; 130001M, BASIC IRK, MEDIUM, Exp. 01/11; 130001M/LAB, BASIC IRK, MEDIUM, Exp. 01/11; 130001S, BASIC IRK, SMALL, Exp. 01/11; 130002L, INCIDENT RESPONSE KIT LG, Exp. 01/11; 130002M, INCIDENT RESPONSE KIT MD. Exp. 01/11; 130002S, INCIDENT RESPONSE KIT SM, Exp. 01/11; 130002S/LAB, INCIDENT RESPONSE KIT, Exp. 01/11; 130018CL/LAB, IRK CBRN SUIT TAPE LARGE/LAB, Exp. 01/11; 130018CM, IRK CBRN SUIT TAPE MED, Exp. 01/11; 130018CM/LAB, IRK CBRN SUIT TAPE MEDIUM/LAB, Exp. 01/11; 130018L/LAB, IRK BASIC SUIT TAPE LARGE/LAB, Exp, 01/11; 130018M/LAB, IRK BASIC SUIT TAPE MEDIUM/LAB, Exp. 01/11; 34180F, 3 SHELF INDUSTRIAL FAK LOGO, Exp. 01/11; 34180FB, 3 SHELF INDUSTRIAL W-BBK/FAK, Exp. 01/11; 34180FCP, 3 SHELF IND.W-CPR/FAK & PUMP, Exp. 01/11; 34180FP, 3 SHELF INDUSTRIAL FAK W/PUMP, Exp. 01/11; 34180FPRF, RE-FILL 180 FAK W/PUMP, Exp. 01/11; 34180LB, 3 SHELF IND W/LINER NO LOGO, Exp. 01/11; 34180LFB, 3 SHELF IND W/LINR & BBK/LOGO, Exp. 01/11; 34180LFBP, 3 SHELF IND W/LINR,BBK/FAK PMP, Exp. 01/11; 34180LFC, 3 SHELF IND W/LINR & CPR/LOGO, Exp. 01/11; 34180LFCP, 3 SHELF IND W/LINR & CPR/PUMP, Exp. 01/11; 34180LFP, 3 SHELF IND W/LINER FAK W/PUMP, Exp. 01/11; 34180RF, REFILL FOR 34-180 KIT, Exp. 01/11; 34180RFP, REFILL FOR 34-180 KIT W/PUMP, Exp. 01/11; 34400F, 4 SHELF INDUSTRIAL FAK LOGO, Exp. 01/11; 34400FBP, 4 SHELF IND.W-BBK/FAK & PUMP, Exp. 01/11; 34400FCP, 4 SHELF IND.W-CPR/FAK & PUMP, Exp. 01/11; 34400FP, 4 SHELF INDUSTRIAL FAK W/PUMP, Exp. 01/11; 34400LB, 4 SHELF IND W/LINER NO LOGO, Exp. 01/11; 34400LF, 4 SHELF IND W/LINER FAK LOGO, Exp. 01/11; 34400LFB, 4 SHELF IND W/LINR & BBK/LOGO, Exp. 01/11; 34400LFBP, 4 SHELF IND W/LN/FAK BBK,PMP, Exp. 01/11; 34400LFC, 4 SHELF IND W/LINR & CPR/FAK, Exp. 01/11; 34400LFCP, 4 SHELF IND W/LINR & CPR/PUMP, Exp. 01/11; 34400LFNP, 4 SHELF IND W/LINER FAK NO TAB, Exp. 01/11; 34400LFP, 4 SHELF IND W/LINER FAK W/PUMP, Exp. 01/11; 34400RF, REFILL FOR 34-400 KIT, Exp. 01/11; 34400RFP, REFILL FOR 34-400 KIT W/PUMP, Exp. 01/11; 34401RF, REFILL FOR 34-401 KIT, Exp. 01/11; 34600F, 600 X LRG INDUSTRIAL FAK LOGO, Exp. 01/11; 34600FC, 5 SHELF IND W/LINR & CPR/PUMP, Exp. 01/11; 34600FP, 600 X LG INDUST PUMP FAK LOGO, Exp. 01/11; 34600RF, REFILL FOR XLG INDUSTRIAL 600, Exp. 01/11; 34601F, 600 X LRG INDUSTRIAL FAK LOGO, Exp. 01/11; 34601RF, REFILL FOR XLG INDUSTRIAL 601, Exp. 01/11; 3536CA, 36 UN CONTRACTOR KIT ANSI FAK, Exp. 01/11; 63157989, LSS CPR EMERGENCY KIT, Exp. 01/11; SF00002012, S0002 16U MT ASPLUNDH TREE FILL, Exp. 01/11; SF00002062, 4909 10U PL LITTLE LEAGUE LOGO/FILL, Exp. 01/11; SF00002071, 3839 6UN COM ED CPR FILL/LOGO, Exp. 01/11; SF00002079, REDICARE MED BAG NO LOGO, Exp. 01/11; SF00002081, 4914 16UN MT CABLEVISION FILL, Exp. 01/11; SF00002087, 4918 16U MT NPL CONSTR WESCO FILL, Exp. 01/11; SF00002089, WEATHERFORD SURVIVAL FANNY PACK KIT, Exp. 01/11; SF00001914, BLUEGRASS TRAUMA BAG, Exp. 01/11; SF00001915, 4853 24UN MT MLGW FILL & LOGO, Exp. 01/11; SF00001925, REFILL FOR GRAINGER #3EWK5 4 SHELF, Exp. 01/11; SF00001932, PUBLIC SAFETY BLS REFILL, Exp. 01/11; SF00001942, 4864 6UN MT STND CPR KIT NYC ENVIROM, Exp. 01/11; SF00002008, 6UN MT CPR NO LOGO INLAD TRUCK&VAN, Exp. 01/11; SF00002010, S0002 16U MT ASPLUNDH TREE FILL, Exp. 01/11; SF00001321, 4714 3 SHELF STD FILL LAWSON LOGO, Exp. 01/11; SF00001322, 4715 4 SHELF LAWSON, Exp. 01/11; SF00001368, 10U RPD LBL TRUCK KIT FILL, Exp.01/11; SF00001371, S0003 16U PL AIRGAS FILL, Exp. 01/11; SF00001411, 0010L 3 SHLF GRAINGER RAPID LB LOGO, Exp. 01/11; SF00001420, 0010L 3 SHLF GRAINGER FILL, Exp. 01/11; SF00001424, 4726 36U MT CHESAPEAKE ENERGY LOGO, Exp. 01/11; SF00001434, S0006 3 SHLF PLANT KIT LONE STAR, Exp. 01/11; SF00001463, 0009L 2 SHLF GRAINGER FILL, Exp. 01/11; SF00001504, 4744 24U MT WELDMARK LOGO/FILL, Exp. 01/11; SF00001528, 4732 24U MT FPL LOGO/FILL, Exp. 01/11; SF00001537, S0006 3 SHLF ELVIN SAFETY FILL, Exp. 01/11; SF00001537, S0006 3 SHLF ELVIN SAFETY FILL, Exp. 01/11; SF00001564, S0004 24U MT GRAINGER FILL, Exp. 01/11; SF00001688, S0006 3 SHLF ARTIC FIRE FILL, Exp. 01/11; SF00001731, 4807 36U MT FILL NJ DOT LOGO/FILL, Exp. 01/11; SF00001740, S0005 36U MT THERMO FISHER FILL, Exp. 01/11; SF00001748, REFILL FOR SF00001685 BIGGE CRANE, Exp. 01/11; SF00001759, 4812 24U MT TEICHERT LOGO/FILL, Exp. 01/11; SF00001818, MJR TRAUMA BAG LIBRA SAFETY FILL, Exp. 01/11; SF00001851, S0004 24U PL GALLS FILL, Exp. 01/11; SF00001853, 4914 16U MT CABLEVISION, Exp. 01/11; SF00001889, REDI CARE LRG. CITY IF JACKSON, Exp. 01/11; SF00000034, 10 UNIT CITY OF MOUNTAIN VIEW FILL, Exp. 01/11; SF00000274, S1051 SSI LOGO FILL2025P 682025PSSI, Exp. 01/11; SF00000302, TRAUMA KIT IN RED FANNY PK 11"X7"X5", Exp. 01/11; SF00000327, S0005 FA LOGO/#36 MT TOTAL TOOL FILL, Exp. 01/11; SF00000334, 4634 16UN MT ARMY CORP FILL/LOGO, Exp. 01/11; SF00000414, S0006 FA LOGO 4 SHELF CABINET HNA, Exp. 01/11; SF00000471, S0905 SSI LOGO FILL H 2200 682200SSI, Exp. 01/11; SF00000474, S0905 SSI LOGO STD 3SH IND 180KIT, Exp. 01/11; SF00000491, PERSON PACK HAGEMEYER FILL, Exp. 01/11; SF00000506, 4643 HIP POCKET KIT W/FRUCON LOGO, Exp. 01/11; SF00000657, S0005 FA LOGO 36U METAL SPI FILL, Exp. 01/11; SF00000660, 24UNIT MTL FP&L FILL, Exp. 01/11; SF00000664, 4712 16UN MT COACH&EQUIPMENT FILL, Exp.01/11; SF00000726, DEL RIO EMERGENCY KIT RED DUFFLE, Exp. 01/11; SF00000763, 150P CABINET NORTH,FIND MRO MODIFIED, Exp. 01/11; SF00000768, S0006 FA LOGO 4SHF USPS FILL, Exp. 01/11; SF00000813, S0006 FEDEX LOGO 2 SHELF FEDEX FILL, Exp. 01/11; SF00000842, SW153 3SHELF HAGEMEYER LOGO L&P FILL, Exp. 01/11; SF00000849, S0006 FA LOGO 3 SHLF ANTHOINE RUBBER, exp. 01/11; SF00000853, REFILL FOR RITZ KIT# 6834600F, Exp. 01/11; SF00000903, SHERIFF FILL IN DUFFLE BAG, Exp. 01/11; SF00000941, 16U MT GRAINGER FILL, Exp. 01/11; SF00000941, 16U MT GRAINGER FILL, Exp. 01/11; SF00000955, S0006 FA LOGO 3 SHELF Z0160 FILL, Exp. 01/11; SF00000972, 4670 WARDS NURSING, Exp. 01/11; SF00001022, S0004 24U PL CITY OF RALEIGH FILL, Exp. 01/11; SF00001068, S075 400 W/LINER QUAD CITY FILL/LOGO, Exp. 01/11; SF00001088, S0006 3SHLF IND WAREHOUSE CARE SAFET, Exp. 01/11; SF00001096, S1022 16U PL HENKELS-MCCOY FILL, Exp. 01/11; SF00001109, SM NYLON BAG SURVIVAL AIRGAS FILL, Exp. 01/11; SF00001113, EMER MED BG 8X8X6 AIRGAS FILL, Exp. 01/11; SF00001129, SW163 3SHLF W/LINER STND FILL/BELFOR, Exp. 01/11; SF00001140, S0003 10UN MT CITY OF MOUNTAIN VIEW, Exp. 01/11; SF00001141, S0004 24UNT MT CITY OF MOUNTAIN VIEW, Exp. 01/11; SF00001214, SURVIVAL BAG GASES PLUS, Exp. 01/11; SF00001240, 4695 16UN MT ORANGE COUNTY FILL/LOGO, Exp. 01/11; SF00001241, 4696 36UN MT ORANGE COUNTY FILL/LOGO, Exp. 01/11; SF00001253, 4683 16U MT NICOR WESCO FILL, Exp. 01/11; SF00001255, AIRGAS PPE POLYBAG FILL, Exp. 01/11; SF00001300, S0006 2 SHLF GRAINGER FILL, Exp. 01/11; SF00001305, S0006 3SHLF ALYESKA PIPELINE FILL, Exp. 01/11. Recall # D-1458-2011;

 

2) Repacked Triad Alcohol Prep Pads (brands include North First Aid Kits, North Safety & Swift, and North by Honeywell) with the following Item #s and names: a) 720374T, Alcohol Prep Pads, Bulk; b) 155818, Alcohol Prep Pads100 Pack; c) 156818, Alcohol Prep Pads 200 Pack; d) 240820, Bulk Alcohol Prep Pads 3000/CS; e)154818, Alcohol Prep Pads 50'S; f) 021047,Alcohol Prep Pads 10/Pack; g) 021057, Alcohol Prep Pads 50/Pack; h) 35224AS, Alcohol Prep Pads 100 Pack, and i) 032525, Alcohol Prep Pads 100 Box. Recall # D-1459-2011

1) All lots;

 

2) a) Exp. 01/11; b) Exp. 01/11; c) Exp. 01/11; d) Exp. 01/11; e) Exp.01/11; f) Exp. 01/11; g) Exp. 01/11; h) Exp. 01/11; i) Exp. 01/11. All lots were manufactured from 01/01/2008 through 01/06/2011.

Recalling Firm: North Safety Products, Inc., Cranston, RI, by email and fax on January 13, 2011.

Manufacturers: H & P Industries, Inc., Hartland, WI;

North Safety Products (dba Swift First Aid), Mexicali, Mexico. Firm initiated recall is ongoing.

Microbial Contamination of Non-Sterile Product: North Safety Kits contain a product component (Triad Alcohol Prep Pads) recalled due to potential bacillus cereus. contamination.

844,868 kits

Nationwide

Dow Corning Q7-2587 and Q7-2587N (both generally referred to as Q7-2587), 30% Simethicone Emulsion USP, Caution for further Manufacturing, Processing and Repacking. AVOID FREEZING. Recall # D-1577-2011

0006069707, 0006149739, 0006069708, 0006196492, 0006069709, 0006196493, 0006069711, 0006196494, 0006069712, 0006196496, 0006080715, 0006212095, 0006080716, 0006212097, 0006085086, 0006215410, 0006085087, 0006215411, 0006099045, 0006215412, 0006099046, 0006221786, 0006099047, 0006221788, 0006104719, 0006223129, 0006104723, 0006245087, 0006104725, 0006245088, 0006104731, 0006245089, 0006125019, 0006245090, 0006125022, 0006276742, 0006125030, 0006276743, 0006125032, 0006276744, 0006125036, 0006283390, 0006125041, 0006285606, 0006135924, 0006285607, 0006135925, 0006296408, 0006135926, 006296410, 0006135927, 0006296412 and 0006314980

Dow Corning Corporation Healthcare Industries Materials Site, Hemlock, MI, by e-mail on December 14, 2010 and December 21, 2010 and by letter on July 20, 2011. Firm initiated recall is ongoing.

Microbial Contamination of Non Sterile Product; mold found in gasket area of drum lid.

558 units

CA, SC, MI, NE, AL, PA, MA, Canada, Mexico, Germany and UK

Non-Sterile Alcohol Prep Pads/Swabs, saturated with 70% v/v Isopropyl Alcohol, distributed under the following labels, sizes and codes: a) PDI Alcohol Prep Pad, MEDIUM, For Professional and Hospital Use, 200 Packets (pads) per box, NDC 10819-3912-1, 10 x 200s, 15 x 200s, 3000 pads; a-c) PDI Item #s B-33901, B33905, B33973, B68870, C29600; b) PDI Alcohol Pads, medium, 100 Individually Foiled Wrapped Pads per box, NDC 10819-3912-3, UPC 0 74887 10050 4; c) PDI Alcohol Prep Pad, LARGE, For Professional and Hospital Use, 100 Packets (pads) per box, NDC 10819-3912-2; d) McKesson Medi-Pak Alcohol Prep Pads - MEDIUM, Non-Sterile, Single Use, Latex-Free, 200 Packets (pads) per box, NDC 68599-5805-1, McKesson Medi-Pak Item #s B-85637, Reorder No. 58-104; e) McKesson Medi-Pak Alcohol Prep Pads - LARGE, Non-Sterile, Single Use, Latex-Free, 100 Packets (pads) per box, NDC 68599-5805-2, McKesson Medi-Pak Item # C42500, Reorder No. 58-304; f) Medichoice Alcohol Prep Pads, MEDIUM, Non-Sterile, Single Use, Latex-Free, 200 Packets (pads) per box, NDC 65517-00021, Medichoice Item #s B91437 and C73400; Reorder # 4725APP101, g) Medichoice Alcohol Prep Pads, LARGE, Non-Sterile, Single Use, Latex-Free, 100 Packets (pads) per box, NDC 65571-00021, Medichoice Item # C73400, Reorder # 4725APP103; h) ProAdvantage Non-Sterile Alcohol Prep Pads, Medium, For Professional and Hospital Use, 200 Packets (pads) per box, NDC 43128-3910-2, ProAdvantage Item #s B34700; i) ProAdvantage Non-Sterile Alcohol Prep Pads, Large, For Professional and Hospital Use,100 packets (pads) per box, NDC 43128-3910-1, ProAdvantage Item #C36100; j) Duane Reade Alcohol Prep Swab,100 Swabs per box, UPC 6 39194 00694 1, Duane Reade Item # B81071; k) ShopRite Alcohol Prep Swabs,100 Swabs per box, UPC 0 41190 20995 4, ShopRite Item # B32071. Recall # D-1579-2011

All lots

Professional Disposables International, Inc., Orangeburg, NY, by letters dated September 16, 2011. Firm initiated recall is ongoing.

Microbial Contamination of Non-Sterile Products: The non-sterile alcohol prep pads/swabs were found to be contaminated with Bacillus cereus based on FDA sampling and analysis.

285,478,600 Packets (Pads)

Nationwide

1) Cramer #111100, Trainer's Kit Refill, packaged in a shipping box labeled with the bar code 3 11960 51530 6, Cramer Products, Gardner, Kansas 66030. The kit includes 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, Triad Disposables, Inc., Brookfield, WI 53045, as well as other components not listed. Recall # D-1580-2011;

 

2) Cramer #111300, Pro Soft Sided Equipped Kit, black nylon bag with a rip-stop front packaged in a shipping box labeled with the bar code 3 11960 64079 4. The kit contains the #111100 Trainers Kit Refill, which includes 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1581-2011;

 

3) Cramer #111700, Deluxe JR Varsity Equipped Kit, black plastic box packaged in a shipping box labeled with the bar code 3 11960 664679 6. The kit contains 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1582-2011;

 

4) Cramer #111800, Junior Soft Sided Equipped Kit, black nylon bag with a rip-stop front packaged in a shipping box labeled with the bar code 3 11960 64379 5. The kit contains the #111100 Trainers Kit Refill, which includes 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1583-2011;

 

5) Cramer #112000, Retail First Aid Kit, white plastic case with a built in handle, containing 3 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1584-2011;

 

6) Cramer #111900, Super Soft Sided Equipped Kit, black nylon bag with a rip-stop front packaged in a shipping box labeled with the bar code 3 11960 64479 2. The kit contains the #111100 Trainers Kit Refill, which includes 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1585-2011;

 

7) Cramer #112600, Varsity Equipped Kit, black steel kit with the Cramer logo packaged in a shipping box labeled with the bar code 3 11960 64779 3. The kit contains the #111100 Trainers Kit Refill, which includes 1 ziplip bag containing 16 pads per kit of Povidone Iodine Prep Pads, 10% Povidone Iodine, USP, Cat. No. 10-3201, NDC 50730-3201-1, as well as other components not listed. Recall # D-1586-2011

1) Lot #s: LUB056, LUK475, LVB093, LVD171, LVI330, LVI332, LVI333, LVI352, LVI354, LVI355, LWB065, or any other lot found to contain Povidone Iodine Pads;

 

2) Lot #s: LUK477, LVC116, LVI335, or any other lot found to contain Povidone Iodine Pads manufactured by Triad

 

3) Lot #s: LVB043, LVB044, LVI345, LUG333, LVH317, or any other lot found to contain Povidone Iodine Pads manufactured by Triad;

 

4) Lot #s: LUK476, LVG261, or any other lot found to contain Povidone Iodine Pads manufactured by Triad;

 

5) Lot #s: LUI403, LVC127, LVC129, LVG280, or any other lot found to contain Povidone Iodine Pads manufactured by Triad;

 

6) Lot #s: LUC118, LVC118, LVL426, LVI336, or any other lot found to contain Povidone Iodine Pads manufactured by Triad;

 

7) Lot #s: LVL427, LVI331, or any other lot found to contain Povidone Iodine Pads manufactured by Triad.

Cramer Products Inc., Gardner, KS, by e-mail letter, fax or telephone on March 28, 2011 and April 7, 2011 and by letter beginning August 15, 2011. Firm initiated recall is ongoing.

Microbial Contamination of Non-Sterile Products: Products contain povidone iodine prep pads which were recalled by their supplier.

4,489 kits

Nationwide, Puerto Rico, Canada, and Bermuda

Fluoxetine Capsules USP, 20 mg, 1000-count bottle, Rx only, NDC 16714-352-02. Recall # D-1605-2011

 Lot #: 1A14009MA, Exp 12/12

Alembic Limited, Formulation Division, Village Panelav, Gujarat, India, by e-mail on September 23, 2011. Firm initiated recall is ongoing.

Adulterated Presence of Foreign Tablet; A capsule of Fluoxetine 40mg was found in a bottle of Fluoxetine 20mg.

1,900 bottles

Nationwide

 

RECALLS AND FIELD CORRECTIONS: DRUGS - CLASS III 

1) Sea Breeze Actives, with 1% Salicylic Acid Acne Treatment, Deep-Clean Astringent, packaged in a) 10-fl. oz. and b) 16-fl. oz bottles, UPC #: a) 827755030201, b) 827755030249. Recall # D-1587-2011;

 

2) Sea Breeze Actives, with 2% Salicylic Acid Acne Treatment, Clear-Pore Astringent, packaged in 10-fl. oz bottles, UPC#: 827755030225. Recall # D-1588-2011

All lots

Marianna Industries Inc., Omaha, NB, by telephone on April 8, 2011 and email on April 12, 2011. Firm initiated recall is complete.

Labeling Illegible: Lot coding and expiration dates were illegible on some containers.

349,164 bottles

MS

 

Red Blood Cells Leukocytes Reduced. Recall # B-1888-11

Unit: GG42474

BloodSource, Inc., Sacramento, CA, by telephone and facsimile on October 31, 2007 and November 7, 2007. Firm initiated recall is complete.

Blood product, collected from a donor whose health history screening was inadequately performed, was distributed.

1 unit

CA

1) Red Blood Cells. Recall # B-1965-11;

2) Platelets Pooled Leukocytes Reduced. Recall # B-1966-11

1) Unit: W088411516204;

2) Unit: W088411401736

Blood Bank of Hawaii, Honolulu, HI, by letter on August 3, 2011. Firm initiated recall is complete.

Blood products, collected from a donor who had traveled to a malarial endemic area, were distributed.

2 units

HI

Red Blood Cells Leukocytes Reduced. Recall # B-2089-11

Unit: 53FF86877

American National Red Cross-Greater Chesapeake and Potomac Region, Baltimore, MD, by electronic mail on May 28, 2011. Firm initiated recall is complete. 

Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed.

1 unit

MD

Platelets Pheresis Leukocytes Reduced. Recall # B-2091-2011

Unit: W035811104673 (part 1); W035811104673 (part 2)

BloodSource, Inc., Mather, CA, by telephone and facsimile on June 20, 2011. Firm initiated recall is complete.

Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed.

2 units

NY, CA

Source Plasma. Recall # B-2092-11

Units: AU0016260; AU0016607; AU0026522; AU0026666

DCI Biologicals Austin, LLC, Austin, TX, by facsimile on June 11, 2011 and electronic mail on July 21, 2011. Firm initiated recall is complete.

Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed.

4 units

CA

Red Blood Cells Leukocytes Reduced. Recall # B-2093-11

Units: W227710071425; W227711401748; W227710071807

Mid-South Regional Blood Center, Memphis, TN, by facsimile on July 6, 2011. Firm initiated recall is complete.

Blood products, collected from a donor who may have traveled to a malarial endemic area, were distributed.

6 units

TN

Red Blood Cells. Recall # B-2094-11

Unit: W227710350917

Mid-South Regional Blood Center, Memphis, TN, by facsimile on January 23, 2011 and electronic mail on July 6, 2011. Firm initiated recall is complete.

Blood product, collected from a donor who may have traveled to a malarial endemic area, was distributed.

1 unit

TN

1) Platelets Pheresis Leukocytes Reduced. Recall # B-2095-11;

2) Platelets Pheresis Leukocytes Reduced Irradiated. Recall # B-2096-11

1) Unit: W04201102731900 (part 3);

2) Units: W04201102731900 (part 1); W04201102731900 (part 2)

Blood Systems, Inc., Lafayette, LA, by telephone and facsimile on June 24, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed.

3 units

LA

Red Blood Cells Leukocytes Reduced. Recall # B-2098-11

Unit: 53G18699

American National Red Cross-Greater Chesapeake & Potomac Region, Baltimore, MD, by electronic mail on June 11, 2011. Firm initiated recall is complete.

Blood product, collected from a donor in which donor suitability was not adequately determined, was distributed.

1 unit

MD

Red Blood Cells Leukocytes Reduced. Recall # B-2123-11

Unit: W089811003430

Inova Health Care Services, Inova Blood Donor Services, Sterling, VA, by telephone on June 20, 2011 and by letter on June 24, 2011. Firm initiated recall is complete.

Blood product, collected from a donor who previously tested repeat reactive for anti-HTLV-I/II was distributed.

1 unit

VA

Red Blood Cells (Apheresis) Leukocytes Reduced. Recall # B-2140-11

Units: 01FH14774 (part 1); 01FH14774 (part 2)

Recalling Firm: The American National Red Cross, West Henrietta, NY, by facsimile on June 15, 2011.

Manufacturer: The American National Red Cross, Albany, NY. Firm initiated recall is complete.

Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed. 

2 units

NY

Red Blood Cells (Apheresis) Leukocytes Reduced. Recall # B-2141-11

Units: W047011066570A; W047011066570B

New York Blood Center, Inc., Westbury, NY, by letter on July 12, 2011. Firm initiated recall is complete.

Blood products, labeled as leukoreduced but did not undergone leukoreduction, were distributed.

2 units

NY

Red Blood Cells. Recall # B-2147-11

Unit: W050911025267

HCSC-Blood Center, Bethlehem, PA, by facsimile and telephone on May 23, 2011, and by follow-up letter on May 24, 2011 and August 9, 2011. Firm initiated recall is complete.

Blood products, collected in a manner that may have compromised the sterility of the collection system, were distributed.

1 unit

PA

Red Blood Cells Leukocytes Reduced. Recall # B-2149-11

Unit: LJ90080

Blood Bank of the Redwoods, Santa Rosa, CA, by letter dated September 14, 2006. Firm initiated recall is complete.

Blood product, collected from a donor whose health history screening was inadequately performed, was distributed.

1 unit

CA

Platelets Pheresis Leukocytes Reduced. Recall # B-2150-11

Unit: LV12851

Blood Bank of the Redwoods, Santa Rosa, CA, by letter dated October 16, 2006. Firm initiated recall is complete.

Blood product, collected in a manner that may have compromised the sterility of the unit, was distributed.

1 unit

CA

Platelets Pheresis Leukocytes Reduced Irradiated. Recall # B-2151-11

Unit: FM95448

Sacramento Medical Foundation, Sacramento, CA, by telephone on December 26, 2006. Firm initiated recall is complete.

Blood product, with a low platelet count, was distributed.

1 unit

CA

Platelets Pheresis Leukocytes Reduced. Recall # B-2152-11

Unit: FM08084

Sacramento Medical Foundation, Sacramento, CA, by telephone on December 19, 2006. Firm initiated recall is complete.

Blood product, with a low platelet count, was distributed.

1 unit

CA

1) Red Blood Cells Leukocytes Reduced. Recall # B-2154-11;

2) Recovered Plasma. Recall # B-2155-11

1) and 2) Unit: LM89139

Sacramento Medical Foundation, Sacramento, CA, by telephone and facsimile on December 13, 2006. Firm initiated recall is complete.

Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed.

2 units

CA, Switzerland

1) Red Blood Cells Leukocytes Reduced. Recall # B-2156-11;

2) Recovered Plasma. Recall # B-2157-11

1) and 2) Units: W038611334841

Suncoast Communities Blood Bank, Inc., Sarasota, FL, by facsimile on July 19, 2011. Firm initiated recall is complete.

Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

2 units

KY, FL

Red Blood Cells Leukocytes Reduced. Recall # B-2158-11

Unit: 16GP90698

American National Red Cross, Central Ohio Region, Columbus, OH, by telephone on July 20, 2011. Firm initiated recall is complete.

Blood product, which was collected from a donor who traveled to a malarial endemic area, was distributed.

1 unit

OH, TX

Red Blood Cells Leukocytes Reduced. Recall # B-2159-11

Unit: W038111061703

Recalling Firm: Florida’s Blood Centers – Lake Park, Palm Beach Gardens, FL, by letter on July 19, 2011.

Manufacturer: Florida’s Blood Centers – Miramar, Miramar, FL. Firm initiated recall is complete.

Blood product, collected from a donor who traveled to a malarial endemic area, was distributed.

1 unit

FL

Red Blood Cells Leukocytes Reduced. Recall # B-2160-11

Unit: 042FR67826

American National Red Cross, Cleveland, OH, by fax on June 21, 2010. Firm initiated recall is complete.

Blood product, collected from a donor who traveled to a malarial endemic area, was distributed.

1 unit

OH

Antihemophilic Factor (Recombinant). Recall # B-2165-11

Unit: TRA09834AB

Baxter Healthcare Corp., Thousand Oaks, CA, by letter dated July 25, 2011. Firm initiated recall is ongoing.

Antihemophilic Factor (Recombinant), manufactured with a potential breach in asceptic processing, was distributed.

1 lot

Nationwide

1) MEDITECH Blood Bank Software MAGIC 5.6 Release. Recall # B-2167-11;

2) MEDITECH Blood Bank Software Client Server 5.6, 6.0 and 6.1. Recall # B-2168-11

1) MAGIC 5.6 Release;

2) Client Server 5.6, 6.0 and 6.1

Medical Information Technology, Inc., Westwood, MA, by e-mail task updates on May 3, 2011. Firm initiated recall is complete.

Software, with a glitch or defect which could lead to an incompatible unit being transfused, was distributed.

1) 391; 2) 298

Nationwide, Canada, UK

1) MEDITECH Blood Bank Software MAGIC 5.63 and 5.64. Recall # B-2169-11;

2) MEDITECH Blood Bank Software Client Server 5.65, 6.05 and 6.06. Recall # B-2170-11

1) Versions 5.63 and 5.64;

2) Client Server 5.65, 6.05 and 6.06

Medical Information Technology, Inc., Westwood, MA, by e-mail task updates on July 15, 2011. Firm initiated recall is ongoing.

Software, with a glitch or defect which could lead to an incompatible unit being transfused, was distributed.

1) 354; 2) 274

Nationwide, Canada, UK, South Africa

Recovered Plasma. Recall # B-2179-11

Unit: LV28691

Blood Bank of the Redwoods, Santa Rosa, CA, by e-mail on March 2, 2006. Firm initiated recall is complete.

Blood product, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

1 unit

Switzerland

Red Blood Cells Leukocytes Reduced. Recall # B -2183-11

Units: LJ42667, LJ65018

Blood Bank of the Redwoods, Santa Rosa, CA, by letter dated March 6, 2006. Firm initiated recall is complete.

Blood products, collected from a donor who traveled to an area considered endemic for malaria, were distributed.

2 units

CA, NC

Red Blood Cells Leukocytes Reduced. Recall # B -2184-11

Unit: LV02722

Blood Bank of the Redwoods, Santa Rosa, CA, by letter dated March 9, 2006. Firm initiated recall is complete.

Blood products, collected from a donor who traveled to an area considered endemic for malaria, were distributed.

1 unit

CA

 

Recovered Plasma. Recall # B-1887-11

Unit: GG42474

BloodSource, Inc., Sacramento, CA, by telephone and facsimile on October 31, 2007 and November 7, 2007. Firm initiated recall is complete.

Blood product, collected from a donor whose health history screening was inadequately performed, was distributed.

1 unit

CA

Platelets Pheresis Leukocytes Reduced, Recall # B-1968-11

Units: FN34838, FN28547, FN33076 (part 1), FN33076 (part 2)

Sacramento Medical Foundation, Sacramento, CA, by telephone on July 31, 2007. Firm initiated recall is complete.

Blood products, which may have reached an unacceptable temperature during shipping, were distributed.

4 units

MA

Source Plasma. Recall # B-2081-11

Units: 5130060159; 5130058994; 5130058656; 5130057508; 5130056394; 5130056031; 5130054812; 5130054626; 5130053693; 5130053442; 5130050399; 5130050190

Octapharma Plasma Inc., Portsmouth, VA, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

12 units

NC

Source Plasma. Recall # B-2082-11

Units: 5130049431; 5130048162

Octapharma Plasma Inc., Portsmouth, VA, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

2 units

NC

Source Plasma. Recall # B-2083-11

Units: 5130034326; 5130033780; 5130033160; 5130032756

Octapharma Plasma Inc., Portsmouth, VA, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

4 units

NC

Source Plasma. Recall # B-2084-11

Units: 5020100789; 5020098770; 5020098368; 5020097725; 5020095595; 5020095268; 5020094695; 5020087185; 5020085855; 5020085376; 5020083461; 5020082789; 5020112706; 5020112071

Octapharma Plasma Inc., Omaha, NB, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

14 units

Austria

Source Plasma. Recall # B-2085-11

Units: 5020061871; 5020085632; 5020083449; 5020080991; 5020080693; 5020078943; 5020073346; 5020072388; 5020071964; 5020070809; 5020069750; 5020068363; 5020067161; 5020064890; 5020078443; 5020074299; 5020064414 

Octapharma Plasma Inc., Omaha, NB, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

17 units

Austria

Source Plasma. Recall # B-2086-11

Units: 5020150946; 5020149431; 5020148684 

Octapharma Plasma Inc., Omaha, NB, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

3 units

Austria

Source Plasma. Recall # B-2087-11

Units: 4570139412; 4570138906; 4570138231; 4570137624; 4570135610; 4570134455; 4570133514; 4570132947; 4570132413

Octapharma Plasma Inc., Charlotte, NC, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

9 units

Austria

Source Plasma. Recall # B-2088-11

Units: 4590125897; 4590125179

Octapharma Plasma Inc., Jacksonville, FL, by electronic mail on July 1, 2011. Firm initiated recall is complete.

Blood products, collected from a donor whose donor suitability was not adequately determined, were distributed.

2 units

NC

Cryoprecipitated AHF. Recall # B-2097-11

Unit: W053311604049

Community Blood Center, Inc., Appleton, WI, by telephone on July 5, 2011. Firm initiated recall is complete.

Blood product, which was not manufactured in accordance to current Good Manufacturing Practices, was distributed.

1 unit

MS

Recovered Plasma. Recall # B-2099-11

Unit: 53G18699

American National Red Cross-Greater Chesapeake & Potomac Region, Baltimore, MD, by electronic mail on June 11, 2011. Firm initiated recall is complete.

Blood product, collected from a donor in which donor suitability was not adequately determined, was distributed.

1 unit

MD

Red Blood Cells Leukocytes Reduced. Recall # B-2145-11

Units: 29KM72106; 29KM72108; 29KM72091; 29KM72092; 29KM72093; 29KM72094; 29KM72097; 29KM72098; 29KM72099; 29KM72101; 29KM72102; 29KM72103; 29KM72104; 29KM72105; 29KM72096; 29KM72107

American National Red Cross Mid Atlantic Region, Norfolk, VA, by facsimile on July 1, 2011 and letter on July 8, 2011. Firm initiated recall is complete.

Blood products, in which the hemoglobin QC was not adequately determined, were distributed.

16 units

VA

Recovered Plasma. Recall # B-2146-11

Unit: 011GG75061

American Red Cross Blood Services, Saint Louis, MO, by facsimile and letter on July 28, 2011. Firm initiated recall is complete.

Blood product, collected from a donor in which donor suitability was not adequately determined, was distributed.

1 unit

CA

Red Blood Cells Leukocytes Reduced. Recall # B-2148-11

Unit: LV41398

Blood Bank of the Redwoods, Santa Rosa, CA, by telephone on August 3, 2006 and by letter dated August 3, 2006. Firm initiated recall is complete.

Blood product, which did not meet the minimum requirement for red cell recovery, was distributed.

1 unit

CA

Red Blood Cells Leukocytes Reduced. Recall # B-2153-11

Unit: LM60977, LM66239

Sacramento Medical Foundation, Sacramento, CA, by telephone on November 10, 2006. Firm initiated recall is complete.

Blood products, which may have been stored at an inappropriate temperature, were distributed.

2 units

CA

Recovered Plasma. Recall # B- 2162-11

Unit: 12GN41187

Recalling Firm: The American National Red Cross, Carolinas Region, Charlotte, NC, by letter on July 16, 2011.

Manufacturer: American Red Cross Blood Services, Asheville, NC. Firm initiated recall is complete.

Blood product, collected from a donor in whom donor suitability was not adequately determined, was distributed.

1 unit

CA

HLA Fusion Software Version, Product Number: FUSPGR, version 2.0.0-SP1, RSSOH1AC-Update.exe, Product: RSSOH1A. Recall # 2166-11

RSSOH1A LOT 003, RSSOH1C LOT 001, RSSOH1C LOT 002, RSSOH1A LOT 004, RSSOH1B LOT 005, RSSOH2B1 LOT 004, RSSOH2B1 LOT 005, RSSOH2B1 LOT 006, RSSOH2B1 LOT 04A

One Lambda, Inc., Canoga Park, CA, by letter on January 17, 2011. Firm initiated recall is ongoing.

HLA Fusion Software, with a glitch or defect, was distributed.

25 units (14 in US)

CA, OK, TX, AL, AR, MO, MN, PA, Canada, UK, France, Germany, Netherlands, Sweden/Finland, Spain/Portugal, Middle East, China, Japan

MEDITECH Blood Bank Software Client Server 6.0 and 6.1. Recall # B-2171-11

Client Server 6.0 and 6.1

Medical Information Technology, Inc., Westwood, MA, by e-mailed task updates on February 11, 2011. Firm initiated recall is complete.

Software, with a defect or glitch, was distributed.

80 units

Nationwide, Canada, UK

1) Liquid Plasma. Recall # B-2180-11;

2) Red Blood Cells Leukocytes Reduced. Recall # B-2181-11;

3) Plasma Frozen. Recall # B-2182-11

1) Units: S195931, S189391;

2) Unit: S115071;

3) Unit: S140331

Community Hospital of the Monterey Peninsula, Monterey, CA, by facsimile on October 12, 2005 or November 21, 2005. Firm initiated recall is complete.

Blood products, collected from a donor with a history of hepatitis associated with mononucleosis, were distributed.

4 units

CA, FL

 

Siemens Axiom Artis U mobile x-ray system Product Usage: Mobile x-ray system.

Model number 10094012; Model number 7008530. Recall # Z-3009-2011

Serial numbers: 20202, 20223, 20231, 20422, 20402, 20435, 21022, 22002, 21005, and 20432; b) Serial numbers: 20146, 21112, 20003, 20115, 20135, 20006, 20113, and 20120

Siemens Medical Solutions USA, Inc., Malvern, PA, by letters dated June 13, 2011. Firm initiated recall is ongoing.

When the heat unit of the angiography system reaches or exceeds 65%, the cool down time display will appear with an acoustic signal. If users ignore the warning and continue the radiation, the tube may be autoprotected when it reaches its temperature limitation causing the X-Ray to lock until the tube cools down. Following a tube auto-protection, an error message "Door is Open" or "Err 421/240: Door open/Switching tube/X-ray lock" will appear.

18 units

Nationwide

OPMI Pentero, OPMI Pentero C, OPMI Pentero 900, OPMI Vario/S8, OPMI Vario/S88, OPMI Neuro Multivision/NC4, OPMI Vario/NC33, OPMI Neuro/NC4, OPMI Neuro/NC4 Ceiling Mount. A surgical microscope and accessories is an AC powered device intended for use during surgery to provide a magnified view of the surgical area. Recall # Z-3275-2011

All-OPMI Pentero

Recalling Firm: Carl Zeiss Meditec, Inc., Dublin, CA, letter dated September 7, 2011.

Manufacturer: Carl Zeiss, Oberkochen, Germany. Firm Initiated recall is ongoing.

Some third party surgical drapes have optically active protective lenses that could affect the ZEISS surgical microscope position information that is passed on to third party navigation systems.

1,677, (741 OPMI Pentero; 739 OPMI Vario and OPMI Neuro 197)

Nationwide

Clinical Chemistry Alkaline Phosphatase, List Number 7D55-21 & 7D55-31. Used for the quantitation of alkaline phosphatase in human serum or plasma. Recall # Z-3278-2011

Units: 71628UN10, Exp. 11/19/2011; 62474UN10, Exp. 11/19/2011; and 08145UN11, Exp. 2/15/2012.

Abbott Laboratories, Inc., Irving, TX, by letter on August 26, 2011. Firm initiated recall is ongoing.

The reagent has the potential to be contaminated with mold, the Cladosporium fungal species.

6,269 units

Nationwide and Internationally

The Trabecular Metal Modular Acetabular System is a modular acetabular cup system consisting of a shell with a preassembled locking ring, a liner, and optional screws. The Shells are available in a variety of sizes and are designed to be used with Trilogy Acetabular System liners. The shell implants are used to replace the hip socket during total hip arthroplasty. The device is indicated for primary or revision surgery for rehabilitating hips damaged as a result on noninflammatory degenerative joint disease (NIDJD) or its composite diagnoses of osteoarthritis, avascular necrosis,protrusio acetabuli, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis and diastrophic variant. The device is intended for either cemented or noncemented use. Part 00-6202-052-21. Recall # Z-3279-2011

Lot #: 61132698

Zimmer Inc., Warsaw, IN, by letter dated July 27, 2011. Firm initiated recall is ongoing.

Product may have a manufacturing non conformance that could prevent the devices from functioning as intended. Specifically, devices in the affected lot may have a locking ring groove depth that prevents the corresponding liner from snapping into the shell. The groove provides the locking ring room to displace when inserting a liner into the shell. There has been one reported incident where the surgeon was unable to lock the liner into the shell because the locking ring groove was too shallow. Investigation revealed that there may be other shells from the same part/lot combination that have the same manufacturing non conformance.

23 units

Nationwide and Australia, Germany, The Netherlands, and Switzerland

Dual Blue-Release Adult Walkers - Wheeled, and Blue Release Junior Walkers with 5 inch Fixed Wheels, Model Numbers: 6240-5F and 6240-JR5F. The recalled product is packaged four (4) units per shipping box. Product Usage: The walkers are intended for people who need additional support to maintain balance or stability while walking. Recall # Z-3280-2011

All 6240-5F and 6240-JR5F wheeled walkers distributed by the firm between 12/15/2010 and 3/4/2011, are subject to recall/correction.

Recalling Firm: Invacare Corp., Elyria, OH, by letter dated April 7, 2011.

Manufacturer: Hebei HealthPlus Medical Device Co, LTD, Handan City, China. Firm initiated recall is ongoing.

The firm is conducting a recall/correction of their adult and junior wheeled walkers due to a component defect. The firm determined that the caster bolt on the wheeled extension was too short to adequately maintain the Nylex fastener. Consequently, over time, this condition incurs the potential for the caster to loosen and detach, causing the wheels to fall off the walker. This scenario would result in instability of the product and poses the potential for serious injury to the user in the event of a fall.

12,764 walkers

Nationwide, PR, Canada, Columbia, and Israel

ADVANTAGE WINDOWS (Workstation) WITH FUNCTOOL OPTION GE Medical Systems, SCS. A software module that provides supplemental information to those images extracted from CT and MR temporal datasets. Recall # Z-3282-2011

Units: 00000156053GE1 00000156054GE9 00000160141GE8 00000160142GE6 00000163510GE1 00000177462GE9 00000177463GE7 00000178185GE5 00000181683GE4 00000188460GE0 00000190791GE4 00000193324GE1 00000197286GE8 00000197290GE0 00000199300GE5 00000211314GE0 00000213647GE1 00000224809GE4 00000224810GE2 00000235766GE3 00000154900GE5 00000156057GE2 00000163515GE0 00000174344GE2 00000176430GE7 00000177464GE5 00000183715GE2 00000190793GE0 00000197289GE2 00000202806GE6 00000211312GE4 00000224811GE0 00000230390GE7 00000230391GE5 00000235769GE7 00000239644GE8 00000B10232002 00000R10048002 00000S10145004 00000Z11048001 00000P10256003 00000S10349006 00000Y11012001 000000U9229001 0000AD11124002 0000AH11070001 00000E10344008 000000F9146004 000000F9146006 000000R9210001 000000R9250003 0000AG11102002 0000ZD10349001 00000F10186001 00000R11013001 00000S11004001 00000T11062001 00000U11056001 000000L9299001 000000Q9349002 000000T9285001 00000C11167002 00000P10137001 00000R10117001 00000H10158001 00000K10140002 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Recalling Firm: GE Healthcare, LLC, Waukesha, WI, byletters dated August 18, 2011.

Manufacturer: GE Medical Systems, SCS, Buc Cedex, France, Firm initiated recall is ongoing.

GE Healthcare has become aware that image orientation of reference series displayed in Functool Diffusion Tensor/FiberTrak protocol on Advantage Workstation may not match with the orientation annotations displayed in the viewport. This issue may impact patient safety.

697

Nationwide and Internationally

Boston Scientific, LATITUDE Patient Management System Communicator, Model 6476, Boston Scientific, LATITUDE RF Communicator & Software, Model 6482. LATITUDE Communicator REF 6468 (only distributed outside the US) The LATITUDE Patient Management system is intended for use to remotely communicate with a compatible Boston Scientific pulse generator and transfer data to a central database. Recall # Z-3283-2011

MODEL SERIAL 6476 195543 6476 195544 6476 195550 6476 195555 6476 195556 6476 195557 6476 195560 6476 195562 6476 195563 6476 195566 6476 195701 6476 195707 6476 195708 6476 195711 6476 195713 6476 195717 6476 195722 6476 195725 6476 195726 6476 195727 6476 195728 6476 195729 6476 195733 6476 195734 6476 195735 6476 195736 6476 195739 6476 195740 6476 195742 6476 195744 6476 195748 6476 195749 6476 195751 6476 195764 6476 195765 6476 195767 6476 195768 6476 195769 6476 195770 6476 195773 6476 195775 6476 195776 6476 195780 6476 195783 6476 195786 6476 195797 6476 195800 6476 195803 6476 195867 6476 195870 6476 195872 6476 195876 6476 195909 6476 195910 6476 195911 6476 195914 6476 195915 6476 195916 6476 195919 6476 195922 6476 195923 6476 195924 6476 195928 6476 195929 6476 195930 6476 195934 6476 195938 6476 195977 6476 195980 6476 196034 6476 196052 6476 196083 6476 196086 6476 196167 6476 196170 6476 196171 6476 196172 6476 196173 6476 196174 6476 196177 6476 196181 6476 196183 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Recalling Firm: Boston Scientific CRM Corp., Saint Paul, MN, by letter dated August 2011.

Manufacturers: Benchmark Electronics Inc, Winona, MN;

Plexus Manufacturing Sdn. Bhd., Penang, Malaysia. Firm initiated recall is ongoing.

A limited number of Model 6476, 6482, and 6468 (Not available in the US) LATITUDE Communicators are unable to authenticate, and thus cannot connect to the LATITUDE System. Customers are instead receiving Latitude Temporarily Unavailable (LTU) message

470 units

Nationwide and United Kingdom, France