The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
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FDA tags Medtronic embolisation device recall as Class IMedtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of ...
Cardiac electrophysiologist Dr. Jonathan Piccini says Medtronic's Define AFib study offers important lessons for other device ...
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Spinal cord stimulators have grown in popularity over the past several years as patients see benefits in the less-invasive ...
Parkinson's disease patients and advocates are marking Friday as the start of a new era for treatment of the illness as a ...
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
Medtronic’s top ventilator executive began fielding pleas from world leaders' representatives five years ago, as pressure ...
For its Pipeline Vantage 021 models, Medtronic is updating the ... The recall doesn’t ask doctors to remove the device from patients who have it implanted. The devices block off blood flow ...
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