Recall of tetracycline capsules, 250 mg and 500 mg by Avet Pharmaceuticals due to failed specs.
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Recall of nizatidine oral solution, 15 mg/mL by Amneal due to NDMA impurity.
Recall of Imager II Angiographic Catheters by Boston Scientific due to catheter tip detachment.
Recall of LeMaitre Over the Wire Embolectomy Catheter by LeMaitre Vascular due to balloon failure.
Recall of Pipeline Flex Embolization Devices by Medtronic due to fracture risk.
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.
Recall of ranitidine tablets, 150 mg by American Health Packaging due to impurity.
Recall of TM-317 PneumoDart-Pneumothorax Needle by Tytek Medical due to needle blockage.
Recall of Up2 and Bow & Arrow by Med Man due to undeclared sildenafil.
Recall of NC Trek RX Coronary Dilatation Catheter and the NC Traveler Coronary Dilatation Catheter by Abbott due to possible balloon malfunction.
Recall of phenytoin oral suspension USP, 125 mg/5 mL by Taro Pharmaceuticals due to dosing issues.
Recall of NC Trek RX and NC Traveler RX coronary dilatation catheters by Abbott Vascular due to failure.
Recall of Comfort Flo humidification systems by Teleflex Medical due to malfunction.
Recall of Stellar 100 and 150 Non-invasive and Invasive Ventilators by ResMed due to alarm failure.
Recall of MiniMed 600 Series insulin pumps by Medtronic due to incorrect dosing.
Recall of Carestation 600 Series Anesthesia Systems by GE Healthcare due to loss of mechanical ventilation.
Recall of CARESCAPE respiratory modules by GE Healthcare due to incorrect values.
Recall of Rompe Pecho EX, CF, and MAX by Efficient Laboratories due to contamination.
Recall of Nopalina flax seed fiber powder and capsules by Salud Natural Entrepreneur due to salmonella.
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