Recall of Flexor Check-Flo Introducers and Flexor Tuohy-Borst Side-Arm Introducers by Cook Medical due an increased chance of separation at a specific point (proximal bond site). If the device separates...
Recall of JET 7 Catheters with Xtra Flex Technology by Penumbra due to risk of unexpected death or serious injury while used for removing clots in stroke patients.
Recall of Baxter SIGMA Spectrum Infusion Pumps with Master Drug Library (Versions 6 and 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software by Baxter Healthcare due to...
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...
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).
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 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 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.
