(Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most ...

Medtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...

Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...

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

In a notice posted to the agency’s website, the FDA noted that on January 30, 2025, Medtronic (MDT) Neurovascular sent all affected customers ...

Feb 24 (Reuters) - The U.S. Food and Drug Administration has approved Medtronic's (MDT.N), opens ... Healthcare & Pharmaceuticalscategory US FDA's top lawyer Hilary Perkins resigns two days ...

Current FDA approval of this adaptive system is for the treatment of Parkinson’s only, not essential tremor, dystonia (a ...

BD, Medtronic and Abbott were among the top 10 medical device manufacturers with the highest number of late reports, the ...

Medtronic is nearing a U.S. launch for its Hugo surgical robot more than three years after receiving approval to release the soft tissue system in Europe. CEO Geoff Martha told investors Tuesday ...

For the one million people diagnosed with Parkinson's disease in the United States, Medtronic plc (NYSE:MDT), a global leader in healthcare technology, proudly announces U.S. Food and Drug ...

Medtronic VP Jason Fontana offered advice for other device developers who might one day be looking for their own NCA.

The U.S. FDA and HHS announced on Tuesday a set of actions and initiatives focused on infant formula to ensure the ongoing quality, safety, nutritional adequacy and resilience of the domestic infant ...