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…
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…
FDA approves new drug to treat influenza-Xofluza (baloxavir marboxil)
Food & Drug Administration approves new drug to treat influenza Xofluza (baloxavir marboxil) Today, the U.S. Food and Drug Administration approved…
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…
ALERT-FDA-DRUG SHORTAGE
Food & Drug Administration Drug Shortage Report Trifluoperazine Hydrochloride Tablets Status: Currently in Shortage Date first posted: 10/02/2018 Therapeutic Categories: Psychiatry 1 mg (NDC…
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 SAFETY COMMUNICATION
Food & Drug Administration SAFETY COMMUNICATION Increased Risk of Corneal Haze Associated with the Raindrop Near Vision Inlay: FDA Safety…
FDA ALERT-MEDWATCH
Food & Drug Administration Alert-MEDWATCH 23 October 2018 MedWatch – The FDA Safety Information and Adverse Event Reporting Program A new MedWatch…