A51

HealthCare Alerts

IntelliVue MX40 patient-worn monitors – increased power consumption and no visual or audible alarms when batteries are low (MDA/2019/025)
Personalized medicine software vulnerability uncovered by Sandia researchers
Vyaire Medical Recalls the enFlow Fluid Warming System Disposable Cartridges Due to Potential Risk of Exposure to Elevated Levels of Aluminum Exposure to Patients
ICS Medical Advisory (ICSMA-19-178-01) Medtronic MiniMed 508 and Paradigm Series Insulin Pumps
Certain Medtronic MiniMed Insulin Pumps Have Potential Cybersecurity Risks: FDA Safety Communication
Dialog+ haemodialysis machines with software versions 9.xx (excluding versions 9.18, 9.1A, 9.1B) – software and hardware upgrade required (MDA/2019/024)
Vervalste verpakkingen kankermedicijn ontdekt
Teleflex Incorporated Announces Worldwide Voluntary Recall of Select Hudson RCI® Sheridan® Endotracheal Tubes
Teleflex Medical Recalls the Hudson RCI Sheridan and Sheridan Endotracheal Tubes Due to Risk of the Sheridan Connector Disconnecting from the Breathing Circuit
Infusion Options Inc. Issues Voluntary Nationwide Recall of All Lots of All Sterile Products Due to Lack of Assurance of Sterility

Events