Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a ...

Medtronic (NYSE:MDT ... The FDA has classified the recall as a Class I, its most serious category, which means continued use of the affected product could result in serious injury or even death.

Medtronic thinks there’s no evidence that anyone using the pumps has been affected in this way, but says it has decided to recall the MiniMed 508 and MiniMed Paradigm series as a precaution and ...

Medtronic has issued a recall for several aortic root cannula devices due to a potential safety risk that could cause loose material to dislodge during use, potentially leading to stroke or death.

The U.S. Food and Drug Administration on Tuesday announced a Class 1 recall — the most serious level — affecting more than 26,000 Medtronic devices used to treat brain aneurysms. The recall ...

The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as Class I following reports of four patient deaths. A Class I recall is ...

Medtronic is seeking regulatory clearance for an insulin pump that could expand its partnership with Abbott. In its application to the Food and Drug Administration, Medtronic is seeking clearance ...

News, December 02, 2022 Alert Another Recall Related to Medtronic HVAD System The controller driveline boot cover of the HVAD system may harden over time, which could delay access to the driveline ...

Medtronic confirmed that its Hugo surgical robot system has been submitted to the FDA for review, alongside the successful completion of a large clinical trial evaluating its performance in multi ...

Medtronic thinks there’s no evidence that anyone using the pumps has been affected in this way, but says it has decided to recall the MiniMed 508 and MiniMed Paradigm series as a precaution and ...