FDA alert-sterile drug products from Pharm D Solutions
19 November 2018 FDA alerts health care professionals and patients not to use sterile drug products from Pharm D Solutions …
ALERT-FDA-Losartan Potassium and Hydrochlorothiazide
Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of…
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…
ALERT-FDA-EPIPEN AUTO-INJECTOR
ALERT-Food & Drug Administration Epipen Auto-Injector FDA alerts patients and health care professionals that some EpiPen auto-injectors may not readily…
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…
FDA-SAFETY COMMUNICATION-ALERT-Alcon CyPass Micro-Stent
UPDATE: Potential Eye Damage from Alcon CyPass Micro-Stent Used to Treat Open-Angle Glaucoma: FDA Safety Communication 24 October 2018 Audience People who…
FDA ALERT-MEDWATCH
Food & Drug Administration Alert-MEDWATCH 23 October 2018 MedWatch – The FDA Safety Information and Adverse Event Reporting Program A new MedWatch…