Drugs
?
-
2010 Drug Recalls
A recall is when a product is removed from the market because it is either defective or potentially harmful. Sometimes a company discovers a problem and recalls a product on its own. Other times a company recalls a product after FDA raises concerns. If you have a medicine that has been recalled, talk to your health care professional about the best course of action. Stores generally have a return and refund policy when a company has announced a recall of its products. The recalls on the list are generally Class I. A record of all recalls (Class I, II, and III) can be found in the FDA Enforcement Report. See also Definitions of Market Withdrawals and Class I, II, and III recalls.
-
2010 Drug Recalls
- December 30, 2010
The Ritedose Corporation Announces the Voluntary Nationwide Recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL Due to Mislabeled Unit Dose Vials - December 30, 2010
Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials - December 23, 2010
American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter - December 22, 2010
Pfizer To Recall One Lot Of Lipitor In The U.S. - December 20, 2010
American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial - December 09, 2010
Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled. - December 09, 2010
McNeil Consumer Healthcare Announces Voluntary Recall Of All Lots Of Rolaids® Extra Strength Softchews, Roldaids® Extra Strength Plus Gas Softchews, And Roldaids® Multi-Symptom Plus Anti-Gas Softchews Sold In The United States - November 29, 2010
Recall of Mylanta and Alternagel Liquid Products - November 24, 2010
Recall of Tylenol Cold Liquid Products - November 15, 2010
Recall of Children's BENADRYL® Allergy FASTMELT® Tablets and Junior Strength MOTRIN® Caplets - November 15, 2010
Recall of ROLAIDS® Extra Strength Softchews - November 04, 2010
Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h - October 27, 2010
Sandoz initiates voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Methotrexate Injection, USP due to the presence of glass particulates - October 23, 2010 WoStandard Homeopathic Company Voluntarily Recalls Hyland’s Teething Tablets
- October 21, 2010
Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h - October 18, 2010
McNeil Consumer Healthcare Announces Voluntary Recall of One Product Lot of TYLENOL® 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico - October 09, 2010 Pfizer Recalls Lipitor (40mg only)
- September 24, 2010
Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa) - July 30, 2010
Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection - July 12, 2010
Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs - July 08, 2010 McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products
- June 24, 2010
P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States - June 15, 2010
Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab™ Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count - June 03, 2010
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk - June 03, 2010
Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility - June 02, 2010
Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences - June 01, 2010
Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL. - May 28, 2010
Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children's Products - May 27, 2010
Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol That May Contain Particulate Matter - May 17, 2010
Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, USP 500 mg/100 mL - May 17, 2010
Voluntary Recall of HYLENEX Initiated - April 30, 2010
McNeil Consumer Healthcare Announces Voluntary Recall of Certain OTC Infants’ and Children’s Products - April 02, 2010
US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles. - March 17, 2010
The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter - January 15, 2010
McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the Americas, UAE, and Fiji
-
-
-
