MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: Select Monoject Flush Prefilled Saline Syringes By...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: Sodium Bicarbonate in 5% Dextrose Injection 150 mEq per...

TOPIC: Surgical Procedure Packs by DeRoyal Industries: Class I Recall - Due to Mislabeled Lidocaine AUDIENCE: Patient, Health...

BD Announces the Voluntary Recall of Specified Lots of ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator in the United States and U.S....

Sagent Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Phenylephrine Hydrochloride Injection, USP, 10 mg/mL Due to Potential...

Meitheal Pharmaceuticals, Inc. (“Meitheal”), announced today that it is voluntarily recalling one (1) lot of Cisatracurium Besylate...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: AUDIENCE: Patient, Health Professional, Risk Manager,...

https://www.fda.gov/drugs/drug-safety-and-availability/fda-alerts-perrigos-voluntary-albuterol-inhaler-recall?utm_medium=email&utm_source...

Fresenius Kabi USA is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /...

If your email program has trouble displaying this email, view it as a web page. Mylan Initiates Voluntary Nationwide Recall of One Lot of...

The forwarded message below is from the FDA with regards to Impax/Amneal Epinephrine auto injectors and device malfunctions.  As most...

Bacitracin for Injection Reason for the Shortage · FDA requested that all manufacturers of bacitracin for injection voluntarily withdraw...