Recalls

Recall of metformin hydrochloride extended-release tablets 500 mg and 750 mg by Amneal due to N-Nitrosodimethylamine (NDMA).

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.

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

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.

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.

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.

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.

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.