Alerts

Recall of Alaris System Hardware by BD (Becton, Dickinson and Company) due to hardware issues that may cause the infusion pump to not operate as expected.

Recall of "Red-E" male enhancement tablet by The Protein Shoppe due to undeclared sildenafil.

Recall of Amiodarone HCl Injection USP and Tranexamic Acid Injection USP by Mylan due to carton label mix-up.

Recall of Always Be Clean Hand Sanitizer and Just Hand Sanitizer by Open Book Extracts due to products labeled to contain methanol.

Certain hand sanitizers labeled with ethanol (ethyl alcohol) or isopropyl alcohol as the primary ingredient have been found to contain subpotent concentrations of these ingredients or to contain methanol or...

Recall of Harmonic Nature Hand Sanitizer by Harmonic Nature S. De R.L.M due to presence of 1-Propanol.

Recall of Zanilast+gel, sanitizer gel by Nanomateriales, SA de CV due to presence of 1-Propanol.

New clinical trial data compelled FDA to remove the boxed warning on canagliflozin products regarding the risk of amputation.

Recall of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer by Asiaticon SA de CV due to undeclared methanol (wood alcohol) and...

Recall of Medfusion 3500 and 4000 Syringe Pumps by Smiths Medical due to risk of medication delivery error.

Recall of Florence Morris antiseptic hand sanitizer by Grupo Asimex De Mexico due to potential presence of undeclared methanol (wood alcohol) and sub – potent ethanol.

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

Recall of all hand sanitizers by Albek de Mexico due to potential presence of undeclared methanol (wood alcohol).

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.