FDA issued a Class I recall for Medtronic's Left Heart Vent Catheters due to safety concerns. 3 injuries reported.

Medtronic recalled its HeartWare ventricular assist device system because of defects that have been tied to four patient deaths, tctmd reports. 1. The FDA commenced the Class 1 recall May 28 after ...

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 ...

(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, sending its ...

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 ...

Oct 8 (Reuters) - A federal advisory panel recommended that Medtronic Inc be allowed to sell a line of implantable heart rhythm devices to a larger pool of patients, based on research showing the ...

A federal appeals court has sided with Medtronic Plc (NYSE:MDT) in a long-running patent dispute, reversing a jury's finding that the company induced infringement of a Colibri Heart Valve LLC patent ...