Alerts

Recall of Yacana Hand Sanitizer by Grupo Yacana Mexico due to potential presence of methanol (wood alcohol) and sub-potent ethanol.

Recall of Organic Goldenseal Root Powder by Maison Terre due to microbial contamination.

Recall of Heparin Sodium Compounded Products by SCA Pharmaceuticals due to incorrect preservative (benzyl alcohol).

Recall of SkinGuard24 – All Day Hand Sanitizer by SG24 due to presence of methanol (wood alcohol).

Ferring Pharmaceuticals US is recalling the following desmopressin nasal spray products for possible superpotency identified during routine product testing.

Recall of ChloraPrep 3 mL applicator by BD due to fungal contamination.

Recall of DDAVP Nasal Spray 10 mcg/0.1mL, Desmopressin Acetate Nasal Spray 10 mcg/0.1mL, STIMATE Nasal Spray 1.5 mg/mL by Ferring Pharmaceuticals US due to superpotency.

Recall of BodyGuard Infusion Administration Sets by CME America due to delivery inaccuracies.

Manufacturers are being required by the FDA to add recommendations about naloxone to prescribing information for all opioids, including buprenorphine and methadone which are used to treat opioid use disorder...

Two lot numbers of dexmedetomidine hydrochloride (Precedex) 200 mcg/50 ml injection have been recalled by Fresenius Kabi USA due to the potential of lidocaine contamination.

Recall of dexmedetomidine hydrochloride injection by Fresenius Kabi due to cross-contamination.

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).