Recall of Pipeline Flex Embolization Devices by Medtronic due to fracture risk.
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Recall of BodyGuard Infusion Pump System by CME America due to possible over and under-infusion.
Recall of phytonadione injectable emulsion, 10 mg/mL single-dose ampules by Dr. Reddy's Laboratories due to ampules breaking/shattering upon opening.
Recall of BodyGuard Microset Infusion Sets for the BodyGuard Infusion Pump System by CME America due to possible under-infusion.
Recall of Active Male by Natural Remedy Store due to undeclared ingredient, tadalafil.
Recall of Alaris System infusion pumps by Becton Dickinson (BD) CareFusion 303 due to software and system errors.
Recall of ketorolac tromethamine injection by Hikma Pharmaceuticals USA due to particulates.
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