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GE Healthcare LLC Giraffe and & T-Piece/Mask Resuscitation Systems: Class 1 Recall - Potential reversal of oxygen/air http://go.usa.gov/4Mc9
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St. Jude Medical, AMPLATZER TorqVue FX Delivery System: Class I Recall - Core Wire May Fracture http://go.usa.gov/4HX4
#FDA -
HAMILTON-T1 Ventilators - Software Versions 1.1.2 & Lower - Class 1 Recall: Possible miscalculation of oxygen http://go.usa.gov/4vB3
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Vycor Viewsite Brain Access System: Class 1 Recall - Unidentified Fiber Found on Device. http://go.usa.gov/4Nsh
#FDA#Safety -
Lactated Ringers and 5% Dextrose Injection, USP, 1000 ML, Flexible Containers: Recall - Due to Non-Sterility http://go.usa.gov/494V
#FDA -
Samsca (tolvaptan): Drug Warning - Potential Risk of Liver Injury http://go.usa.gov/4KRw
#FDA -
Bausch and Lomb 27G Sterile Cannula Packed in Amvisc/Amvisc Plus OVDs: Recall, Cannulas May Leak, Detach From Syringe http://go.usa.gov/4Z3W
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Metal-on-Metal Hip Implants: Safety Communication - Metal release will cause some tiny metal particles to wear off... http://go.usa.gov/4bfT
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December 2012 Safety Labeling Changes includes 42 products with revisions to Prescribing Information http://go.usa.gov/4bwd
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Ferrous Sulfate Tabs 325 mg Labeled as Rugby Natural Iron: Recall - Bottles May Contain Meclizine HCl 25 mg Tabs http://go.usa.gov/4b4e
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Mobius brand Mitosol Kit for Ophthalmic Use: Recall -May contain a strain of yeast on one or more parts in the kit http://go.usa.gov/4xFw
#FDA -
Zolpidem Containing Products: Drug Safety Communication - FDA Requires Lower Recommended Doses http://go.usa.gov/4cUA
#FDA -
Fisher and Paykel Healthcare Reusable Breathing Circuit: Class I Recall - Pinholes in Tubes http://go.usa.gov/gSjC
#FDA -
Praxair Inc., Grab ‘n Go Vantage Portable Oxygen Cylinder Units: Class I Recall - Risk of Fire Inside Cylinder http://go.usa.gov/gtNF
#FDA -
GE Healthcare T-Piece Circuits for the Giraffe and Panda Resuscitation Systems: Class I Recall – http://go.usa.gov/gFFP
#FDA -
Zimmer Spine - PEEK Ardis Inserter: Class I Recall – Risk of Implant Breakage http://go.usa.gov/gFDj
#FDA -
Ventlab Adult and Pediatric Manual Resuscitators: Recall-Valve Leak Prevents Flow of Air/Oxygen to Patient http://go.usa.gov/gAHT
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Bunnell Life Pulse High-Frequency Ventilator Patient Circuits: Recall- Melted Insulation Can Cause Sparking and Smoke http://go.usa.gov/gAH3
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Medtronic Drug Infusion Pumps: Recall - Intermittent or Permanent Pump Motor Stall http://go.usa.gov/gAAz
#fda -
Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg: Recall - Potential for Oversized Tablets http://go.usa.gov/gAAP
#fda
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