Alerts

FDA issued recall of bevacizumab 1.25mg/0.05mL 31G injectable by AmEx Pharmacy due to reported defective delivery system.

Sudden discontinuation or rapid dose reduction of prescription opioids in patients who are physically dependent on these medications can cause serious harm including psychological distress, serious withdrawal symptoms, suicide, and...

FDA issued recall of Miller balloon atrioseptostomy catheter and Fogarty dilation atrioseptostomy catheter by Edwards Lifesciences due to balloon deflation, fragmentation and detachment Issue.

FDA issued recall of Fentanyl Transdermal System by Alvogen due to product mislabeling.

FDA issued recall of Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP by Torrent Pharmaceuticals due to impurity.

FDA issued recall of Spine & Trauma 3D Navigation by Brainlab AG due to inaccurate display.

FDA issued recall of aphrodisiac capsules by SD Import due to undeclared sildenafil.

Prinston Pharmaceutical Inc. recalled tablets of irbesartan and irbesartan co-formulated with hydrochlorothiazide. The recall affects 1 lot of irbesartan and 7 lots of irbesartan-hydrochlorothiazide. One of the raw ingredients, irbesartan...

More manufacturers have recently recalled their valsartan products.

FDA issued recall of o_two e700, e600 and e500 automatic transport ventilators by O-Two Medical Technologies due to fire risk.