Alerts

Recall of Fixed Core Wire Guides by Cook Medical due to manufacturing error.

Sunstar Americas Inc. (SAI) issued a voluntary recall of specific lots of chlorhexidine gluconate 0.12% oral rinse with an expiration date between 6/30/2022 – 9/30/2022 due to possible bacterial contamination...

Recall of Chlorhexidine Gluconate Oral Rinse USP, 0.12% by Lohxa due to microbial contamination.

Recall of Trevo XP ProVue Retriever by Stryker Neurovascular due to failure potential.

Some metformin hydrochloride extended-release (ER) products, including brand-name Fortament and Glumetza, may contain low concentrations of a probable human carcinogen called N-nitrosodimethylamine (NDMA).

Recall of Rashkind Balloon Septostomy Catheters by Medtronic due to quality issues.

Recall of metformin HCl extended release tablets, USP 750 mg, by Nostrum Laboratories due to n-nitrosodimethylamine (NDMA).

FDA issued a Drug Safety Communication recommending against non-steroidal anti-inflammatory drug (NSAID) use in pregnant women at 20 weeks or later due to serious and rare kidney complications in an...

FDA issued an update to the benzodiazepine drug class boxed warning to emphasize the serious risk of addiction, abuse, and withdrawal reactions.

FDA recently issued a MedWatch alert warning consumers about serious harm with diphenhydramine when taken in amounts exceeding the recommended dose. The warning is in response to recent reports of...

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

Recall of licensed hand sanitizers packaged in 0.84 fluid ounce pouches by Ashtel Studios due to misbranding; they resemble food and drink container pouches.

Recall of Alaris System Pump Module and Pump Module Door Assembly Replacement Kits by Becton Dickinson CareFusion 303 due to potential for stuck or unresponsive keys.

Recall of Cleaner Hand Sanitizer By DMM VISSION due to undeclared methanol.

Recall of metformin hydrochloride for extended-release oral suspension by Sun Pharmaceutical Industries due to n-nitrosodimethylamine (NDMA).

Acella LLC is recalling specific lots of 15 mg and 120 mg levothyroxine (T4) and liothyronine (T3) thyroid tablets, USP (NP Thyroid) due to sub potency identified during testing.

Recall of NP Thyroid (Thyroid Tablets USP) by Acella Pharmaceuticals due to subpotency.

Recall of Alaris Syringe and Alaris PCA Modules by BD CareFusion 303 (Becton, Dickinson and Company) due to potential incorrect display of syringe types and/or sizes.

Recall of Alaris System Infusion Pumps by BD CareFusion 303 (Becton, Dickinson and Company) due to damaged inter-unit interface connectors, loose or missing battery screws and a broken upper and...

Recall of Alaris System PC Unit and PC Unit Front Case Keypad Replacements Kits by BD (Becton, Dickinson and Company) due to risk of stuck or unresponsive keys.

Recall of M Hand Sanitizer by Medek due to possible methanol (wood alcohol) and subpotent ethanol levels.

Recall of Nature-Throid and WP Thyroid By RLC Labs due to sub potency.

Recall of Leafree Instant Hand Sanitizer - Aloe Vera by CorgioMed due to product labeled as edible alcohol.

Recall of bio aaa Advance Hand Sanitizer by AJR Trading due to possible presence of methanol.