ALERT-UPDATE-DEFIBRILLATOR FAILURE LOCK UP LIFEPAK 15-STRYKER
28 FEBRUARY 2019 DE FAAKTO ALERT ALERT INTELLIGENCE U.S. FOOD & DRUG ADMINISTRATION UPDATE DEFIBRILLATOR FAILURE LOCK UP-LIFEPAK 15-STRYKER The FDA has identified this…
Recall of Vecuronium Bromide for Injection
Alert from U.S. Food & Drug Administration 08 January 2019 Sun Pharmaceutical Industries, Inc. Issues Voluntary Nationwide Recall of Vecuronium Bromide…
Alert-FDA-Mylan-Valsarten, Amlodapine & Valsarten, Hydrochlorothiazide & Valsarten Tablets-Recall
Alert From the U.S. Food & Drug Administration Mylan-Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide…
Alert-FDA-Infant Ibuprofen-Recall
The U.S. Food & Drug Administration has issued an Alert-Recall Tris Pharma Issues Voluntary Nationwide Recall of Infants’ Ibuprofen Concentrated…
Alert-FDA-Safety Recall-Valsarten, Amlodipine, Valsarten & Hydrochlorothiazide
U.S. Food & Drug Administration Safety Alert recall-Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide…
Recall of Puriton Eye Relief Drops
From the U.S. Food & Drug Administration Kadesh Incorporation Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops Due to…
ALERT-FDA-DRUG SHORTAGE-DIAZEPAM & VOLUNTARY RECALL ORTHO-NOVUM
From the Food & Drug Administration Diazepam Injection Status: Currently in Shortage Date first posted: 09/22/2017 Therapeutic Categories: Neurology Hospira Inc. 10 mg/2 mL (5…
MEDICAL-ALERT-FDA-Multiple Safety
MEDICAL ALERT Food & Drug Administration 1. Maquet Datascope Corp./Getinge Group Recalls the Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon…
Alert FDA Drug Safety-Recall
From the U.S. Food & Drug Administration Irbesartan Tablets Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP 75…