Recall of metformin hydrochloride extended-release tablets 500 mg and 750 mg by Amneal due to N-Nitrosodimethylamine (NDMA).
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Recall of StealthStation Auto-Registration Feature by Medtronic due to inaccuracies.
Recall of metformin hydrochloride extended-release tablets 500 mg by Apotex due to N-Nitrosodimethylamine (NDMA).
Recall of HeartWare HVAD Pump Outflow Graft and Outflow Graft Strain Relief by Medtronic due to potential failure.
Recall of NP Thyroid (Thyroid Tablets) by Acella due to super potency.
Recall of KORE ORGANIC Watermelon CBD Oil by Summitt Labs due to high levels of lead.
Recall of Python Embolectomy, BARD Embolectomy, and OTW Latis cleaning catheters by Applied Medical due to potential separation.
Recall of finasteride plus 1.25mg by MasterPharm due to undeclared minoxidil.
Recall of lactated ringer's injection, USP by ICU Medical due to particulate matter.
Recall of Langston dual lumen catheter by Vascular Solutions due to risk of separation.
The FDA cautions against use of hydroxychlorquine and chloroquine outside of a hospital setting or clinical trial.
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.
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