Alerts

Recall of several hemp oil products from InHe Manufacturing and MHR Brands due to potential lead.

Recall of GlideScope Core One TouchSmart Cable (“OneTouch cable”) by Verathon due to potential image loss.

Recall of hand sanitizers by 4e Brands North America due to presence of undeclared methanol.

Recall of metformin hydrochloride extended-release tablets USP, 500 mg and 1000 mg by Lupin Pharmaceuticals due to N-Nitrosodimethylamine (NDMA).

Recall of daptomycin for injection, 500 mg/vial by Mylan due to presence of particulate.

Recall of metformin hydrochloride extended-Release tablets USP 750 mg by Granules Pharmaceuticals due to N-Nitrosodimethylamine (NDMA).

Recall of Arrow AutoCAT2 and AC3 Optimus Intra-Aortic Balloon Pump (IABP) Series by Arrow International due to possible break down.

Recall of Children's Robitussin Honey Cough and Chest Congestion DM and Children's Dimetapp Cold and Cough by GSK due to dosing cups missing graduation markings.

FDA released a safety alert regarding the possible reduced antiviral activity of remdesivir when administered concomitantly with hydroxychloroquine sulfate or chloroquine phosphate.

Recall of Ovation iX Abdominal Stent Graft Systems by Endologix due to polymer leaks.

Recall of metformin hydrochloride extended-release tablets USP 500 mg by Lupin Pharmaceuticals due to N-Nitrosodimethylamine (NDMA).

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

Recall of metformin hydrochloride extended-release tablets USP, 500 mg by Marksans due to N-Nitrosodimethylamine (NDMA).

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.

The FDA cautions against use of hydroxychlorquine and chloroquine outside of a hospital setting or clinical trial.