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 ...

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 ...

Dozens of patients were put at risk after two of the UK's leading transplant centres continued fitting a heart device - despite knowing of concerns it had a higher mortality rate than its rival ...

Medtronic has recalled certain DLP Left Heart Vent Catheters due to a defect that could cause serious injury or death. The recall applies to model numbers 12110, 12113 and 12115 with UDI-DIs ...

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 ...

CHICAGO (Reuters) - A Minnesota state court judge has dismissed a batch of lawsuits against Medtronic Inc stemming from the October 2007 recall of the medical device maker's Sprint Fidelis ...

Medtronic this week launched its OmniaSecure defibrillation lead in the U.S., describing it as the world's smallest.

(Reuters) -Medical device maker Medtronic topped Wall Street estimates for second-quarter profit and revenue on Tuesday, driven by strong demand for its heart disease and diabetes devices. Investor ...