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", ...
MassDevice6 天
Medtronic recalls embolization device after reported deaths
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Medtronic ventilators helped save lives during the pandemic, so why is the company shutting ...
Medtronic’s top ventilator executive began fielding pleas from world leaders' representatives five years ago, as pressure ...
MedTech Dive5 天
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 ...
Medical Dialogues4 天
Recall of Medtronic embolization devices classified as most serious by USFDA
Medtronic's recall of embolization device has been classified most serious by the U.S. Food and Drug Administration (USFDA), ...
Medical Device Network on MSN5 天
FDA tags Medtronic embolisation device recall as Class I
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
Star Tribune5 天
Medtronic recalls aneurysm-treating device linked to four deaths
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 ...
'Breakthrough' deep brain stimulation device for Parkinson's to make clinical debut
Parkinson's disease patients and advocates are marking Friday as the start of a new era for treatment of the illness as a ...
BioWorld5 天
Latest device recalls include Medtronic embolization devices
The U.S. FDA has posted several class I recalls in recent days, including a removal of one model of the Medtronic Vascular’s ...
Yahoo Finance5 天
Medtronic recalls embolization devices tied to 17 injuries, 4 deaths
Medtronic has recalled embolization devices collectively linked to reports of 17 injuries and four deaths, the Food and Drug Administration said Tuesday. The recall has two elements: Medtronic is ...
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 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 ...