Cybersecurity vulnerabilities in certain Medtronic CareLink programmers are at the center of the recent voluntary recall. (This story has been updated with an FDA statement.) See Also: A Legal ...

The FDA issued a Class I recall — the most serious recall classification — for some of Medtronic’s cardiac resynchronization therapy and implantable cardioverter defibrillators. Here are four things ...

The U.S. Food and Drug Administration (FDA) said it is aware that Medtronic Plc (NYSE: MDT) has notified customers to remove certain Left Heart Vent Catheters from use and sale, citing safety concerns ...

The Food and Drug Administration has issued a Class I recall of about 15,000 guidewires on various Medtronic heart devices, saying the defective coating on the wires could cause serious injury or ...