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...
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 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...