Numerous medical devices sold in the United States are subject to active recalls. If you have a medical device that is subject to an active recall, it will be important to make sure you know what this ...

According to the U.S. Food and Drug Administration records, in an average year over 2,500 medical device recalls are issued in the United States. Some of these recalls simply require checking the ...

Fresenius has issued a software release to address issues that could interrupt treatment with its Ivenix large volume pumps.

Illinois Sen. Dick Durbin and Rep. Jan Schakowsky want an electronic format for medical device makers to quickly and transparently report recall information to federal regulators to improve what they ...

Zoll Circulation is recalling its AutoPulse NXT Resuscitation System due to a failure code that can result in stopped or inadequate chest compressions. The malfunction may delay lifesaving CPR and ...

An urgent recall has gone out for a popular medical device used by millions of Americans with diabetes. The US Food and Drug Administration (FDA) has revealed that over two million blood glucose ...

Receiving a recall notice for a medical device can be deeply unsettling for Louisiana residents who rely on these devices daily—whether for sleep support, pain management, or mobility—news of a recall ...

Medical device firm managers trust physicians to screen out defects in lieu of recalls, a study conducted by Indianapolis-based Indiana University and Minneapolis-based University of Minnesota ...

Defective medical devices can present serious—and sometimes life-threatening—risks for patients. As a patient, you never expect a medical implant to cause you harm. You expect the manufacturer to ...