FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
Medtronic slips after FDA notice on product recall (update)
Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...
FDA tags Medtronic embolisation device recall as Class I
Medtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
MedTech Dive27 分钟
Medtronic recalls embolization devices tied to 17 injuries, 4 deaths
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
FDA issues Medtronic embolization device recall and correction notice
In a notice posted to the agency’s website, the FDA noted that on January 30, 2025, Medtronic (MDT) Neurovascular sent all affected customers ...
MedTech Dive1 天
Top device firms report safety data late: BMJ
BD, Medtronic and Abbott were among the top 10 medical device manufacturers with the highest number of late reports, the ...
Medical Device Network on MSN1 天
FDA adds haemodialysis tubes to shortage list amid supply issues
The US Food and Drug Administration (FDA) has added haemodialysis bloodlines to its medical device shortages list amid supply ...
Reuters23 天
US FDA approves Medtronic's medical device for Parkinson's disease
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 ...
News-Medical.Net on MSN16 天
Medtronic receives FDA approval for BrainSense Adaptive DBS technology
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 ...
Yahoo Finance29 天
Medtronic nears FDA submission for Hugo robot
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 ...
Nasdaq23 天
Medtronic earns U.S. FDA approval for the world's first Adaptive deep brain stimulation ...
The U.S. FDA approval also includes the Medtronic BrainSense™ Electrode Identifier (EI), which helps reduce patient time spent in clinic to program their DBS settings. By using EI, clinicians ...