recall

ALERT-DEFIBRILLATOR FAILURE LOCK UP LIFEPAK 15-STRYKER

DE FAAKTO ALERT 02 FEBRUARY 2019 ALERT INTELLIGENCE U.S. FOOD & DRUG ADMINISTRATION DEFIBRILLATOR FAILURE LOCK UP-LIFEPAK 15-STRYKER Stryker Launches Voluntary Field Action…

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…