medical device recall

HeartWare Ventricular Assist Devices Recalled for Defective Batteries

The batteries in HeartWare Ventricular Assist Devices can lose power prematurely due to faulty cells. This defect could cause serious health consequences or even death.

Battery Packs Used on Patient Monitors Recalled for Fire Risk

Medtronic Respiratory & Monitoring Solutions is recalling certain battery packs due to a manufacturing...

Dialog+ Hemodialysis Systems Recalled for Defective Conductivity Sensors

Braun Medical Inc. is recalling Dialog+ Hemodialysis Systems because defective conductivity sensors can prevent the device from working properly. The recall includes 1,033 units of the systems, which were distributed from June 2013 to October 2015.

Dexcom Inc. Recalls Glucose Monitoring System Receivers for Alarm Failure

Dexcom, Inc. is recalling three models of glucose monitoring systems because the audible alarm...

FDA Issues Class I Recall for Dräger’s Emergency Transport Ventilators

Dräger Medical Inc. is recalling certain Dräger Oxylog Emergency Transport Ventilators because a system error...

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Medical Ventilators Recalled due to Defective Battery

A faulty battery in two ventilators by Dräger Medical has prompted the U.S. Food...

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FDA Proposes Ban on Electrical Stimulation Devices

TDK Releases New Output Voltage Power Supplies for Medical/Industrial Devices