Alerts

The FDA has not approved any treatments or vaccines for COVID-19 as of yet. The only way to obtain an approved test for COVID-19 or for any type of treatment...

Recall of phytonadione injectable emulsion, 10 mg/mL single-dose ampules by Dr. Reddy's Laboratories due to ampules breaking/shattering upon opening.

Recall of BodyGuard Microset Infusion Sets for the BodyGuard Infusion Pump System by CME America due to possible under-infusion.

Recall of Active Male by Natural Remedy Store due to undeclared ingredient, tadalafil.

FDA issued a warning about the risk of transmitting multidrug resistant organisms (MRDOs) via fecal microbiota transplant (FMT). Patients considering FMT for C difficile should discuss the associated risks with...

FDA announced that montelukast (Singulair) would require a boxed warning and Medication Guide related to increased risk for neuropsychiatric events.

Recall of Alaris System infusion pumps by Becton Dickinson (BD) CareFusion 303 due to software and system errors.

Recall of ketorolac tromethamine injection by Hikma Pharmaceuticals USA due to particulates.

Recall of ranitidine tablets, 150 mg by American Health Packaging due to impurity.

Recall of TM-317 PneumoDart-Pneumothorax Needle by Tytek Medical due to needle blockage.

Recall of Up2 and Bow & Arrow by Med Man due to undeclared sildenafil.

Recall of NC Trek RX Coronary Dilatation Catheter and the NC Traveler Coronary Dilatation Catheter by Abbott due to possible balloon malfunction.

Recall of phenytoin oral suspension USP, 125 mg/5 mL by Taro Pharmaceuticals due to dosing issues.

Recall of NC Trek RX and NC Traveler RX coronary dilatation catheters by Abbott Vascular due to failure.

Recall of Comfort Flo humidification systems by Teleflex Medical due to malfunction.

Recall of Stellar 100 and 150 Non-invasive and Invasive Ventilators by ResMed due to alarm failure.

Health care providers should stop prescribing and dispensing lorcaserin immediately.

Recall of MiniMed 600 Series insulin pumps by Medtronic due to incorrect dosing.

Recall of Carestation 600 Series Anesthesia Systems by GE Healthcare due to loss of mechanical ventilation.

Recall of CARESCAPE respiratory modules by GE Healthcare due to incorrect values.

Recall of Rompe Pecho EX, CF, and MAX by Efficient Laboratories due to contamination.

FDA Updates Warnings for Bowel Problems Associated with Clozapine

Recall of Nopalina flax seed fiber powder and capsules by Salud Natural Entrepreneur due to salmonella.

Recall of Galemed Babi.Plus pressure relief manifolds (PRM) by Teleflex due to dislodged valve.