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Non-aspirin Nonsteroidal Anti-inflammatory Drugs (NSAIDs): Drug Safety Communication
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Lifesaver Single Patient Use Manual Resuscitator by Teleflex Hudson RCI: Class I Recall
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Unapproved Prescription Ear Drop (Otic) Products: Not FDA Evaluated for Safety, Effectiveness and Quality
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Codeine Cough-and-Cold Medicines in Children: Drug Safety Communication
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FLOW-i Anesthesia Systems by Maquet: Class I Recall
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Daytrana Patch (methylphenidate transdermal system): Drug Safety Communication
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Covidien Shiley Neonatal and Pediatric Tracheostomy Tubes by Medtronic: Recall – Tubes Formed With Wider
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HeartWare Ventricular Assist System: Class I Recall – Updated with Multiple Reasons for Recall
[Posted 06/22/2015] AUDIENCE: Risk Manager, Nursing, Cardiology ISSUE: Heartware recently conducted multiple recalls for this device. They are all outlined in the firm’s June 8, 2015 press release. The FDA will update this page as new information becomes available. HeartWare Ventricular Assist System – Damaged Alignment Guides / Connection Pins May Cause Pump to Stop…
M/L Taper with Kinectiv Technology Prosthesis by Zimmer: Class I Recall
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