Medication Safety Officers Society
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The Abbott HeartMate Touch Communication System is being recalled due to the risk of unintended communication with the HeartMate System Controller resulting in pump stop of the HeartMate 3 Left Ventricular Assist Device.
Windstone Medical Packaging recalls kits (Lower Extremity, Ocular, Closure) due to sterility concerns linked to Nurse Assist's November 6, 2023, recall.
Cardinal Health is recalling Monoject Luer-Lock and Enteral Syringes due to recognition and compatibility issues with certain enteral syringe feeding pumps.
If the bonded spiral wrap detaches, it can compromise the structural integrity, functionality, or cause blockage, stoppage, or leaks in the breathing circuit.
Baxter Healthcare is recalling the ExactaMix Pro 1200 and Pro 2400 for a software error causing potential over-delivery of ingredients in the final solution.
EVair Air compressors recalled due to increased formaldehyde emissions at high temperature and low gas flow conditions when used with certain ventilators.
Learn more about recommendations for patients who are considering a Hintermann Series H3 TAR system or who have one; recommendations for health care providers.
Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA S
In direct response to the Nurse Assist, LLC voluntary recall of pre-filled syringes and other sterile water products, Avanos Medical, Inc. (NYSE: AVNS) voluntarily recalled specific lots of MIC* Gastric – Jejunal Feeding Tube Kits on Jan. 16, 2024. These kits include Nurse Assist supplied syringes,
Brassica Pharma Pvt. Ltd. is voluntarily recalling Eye Ointment products listed in the table below with expiration date ranging from February 2024 to September 2025. The products are being recalled due to lack of sterility assurance at the facility noted during an inspection conducted by the Food an
Do not use smartwatches or smart rings to measure blood glucose. They are not authorized by the FDA. Using them could result in inaccurate blood glucose measurement, which can lead to serious injury or death if used to make medical decisions. Only use FDA-authorized devices to measure blood glucose.