Alerts

Recall of ceftazidime injection by B. Braun due to failed specs.

International Laboratories, LLC is voluntarily recalling lot # 117099A of clopidogrel 75 mg tablets in 30-count bottles.

Recall of ketorolac tromethamine injection, 30mg, 60mg by Fresenius Kabi due to particulate matter.

Recall of tetracycline capsules, 250 mg and 500 mg by Avet Pharmaceuticals due to failed specs.

Recall of nizatidine oral solution, 15 mg/mL by Amneal due to NDMA impurity.

Humans should never ingest any drug intended for use in animals, as it can cause serious harm. Drugs intended for animals cannot be substituted for those intended for humans.

Updated findings suggest that COVID-19 may be transmitted through FMT.

Recall of Imager II Angiographic Catheters by Boston Scientific due to catheter tip detachment.

Recall of LeMaitre Over the Wire Embolectomy Catheter by LeMaitre Vascular due to balloon failure.

FDA requested all manufacturers of ranitidine products to immediately withdraw their products from the US market.

Animal drugs are not interchangeable with human drugs.

Recall of Pipeline Flex Embolization Devices by Medtronic due to fracture risk.

Recall of BodyGuard Infusion Pump System by CME America due to possible over and under-infusion.

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.