by Kristy Miller | Mar 18, 2025 | Recall
Embolization Device Recall and Correction: Medtronic Removes Unused 027 Compatible Pipeline Vantage Embolization Device with Shield Technology, Updates Use Instructions for 021 Compatible Pipeline Vantage Embolization Devices due to Increased Risk of Incomplete Wall...
by Kristy Miller | Mar 1, 2025 | Recall
Power Assist Device Recall: Max Mobility/Permobil Removes SpeedControl Dial Component Used with SmartDrive MX2+ Power Assist Device Due to Risk for Motor to Be Unresponsive to the User Max Mobility/Permobil is recalling the SpeedControl Dial component used with the...
by Kristy Miller | Feb 17, 2025 | Recall
The U.S. Food and Drug Administration (FDA) is alerting patients who use diabetes devices, as well as their caregivers and health care providers, of a safety concern regarding diabetes devices, such as continuous glucose monitors (CGMs), insulin pumps and automated...
by Kristy Miller | Feb 17, 2025 | Recall
Continuous Ventilator Correction: Baxter Healthcare Corporation Issues Correction for Life2000 Ventilator due to a nonconforming battery charger, which triggers a battery alarm and renders the ventilator inoperable Baxter Healthcare Corporation is correcting the...
by Kristy Miller | Feb 17, 2025 | Recall
Oxygen Concentrator Recall: JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD Removes JMC5A Ni/TruAire-5 Oxygen Concentrator due to the devices spontaneously catching fire JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD is recalling devices due to incidents of device...
by Kristy Miller | Dec 22, 2024 | Recall
Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use ICU Medical is recalling some CSB batteries that are intended for use...
