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HealthCare Alerts

Philips Respironics Recalls Certain V60 and V60 Plus Ventilators for Expired Adhesive that May Cause Ventilator to Stop Working With or Without an Alarm
Medical Recall - Update: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks
Field Safety Notices from Abbott, DTR Medical, Getinge, Haemonetics, Hillrom, Illumina, Intuitive, LeMaitre, Medtronic, Philips, Shenzhen Ma
FDA Warns Against Use of Renuvion/J-Plasma Device for Certain Aesthetic Procedures: FDA Safety Communication
Philips Respironics CPAP, BiPAP, and Ventilator Recalls: Frequently Asked Questions
Baxter recalls SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9) due to the risk of not alarming for repeated upstream occlusion events
Update: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication
Security vulnerabilities identified in the Axeda agent and Axeda Desktop Server
Medtronic Recalls TurboHawk Plus Directional Atherectomy System Due to Risk of Tip Damage During Use
Field Safety Notices: 28 February to 4 March 2022

Events