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", ...
Medical Device Network on MSN1d
FDA tags Becton, Dickinson and Company infusion software recall as Class I
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
FDA adds hemodialysis devices to shortage list amid B. Braun disruption
The disruption is expected to impact patient care, may require adjustments to the management of hemodialysis patients and ...
Colombian Navy personnel indicted in plot to help narcos spy on coast guard ships
Colombian Navy workers are accused of helping drug traffickers place tracking devices aboard Colombian Navy vessels.
GlobalData on MSN3d
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 ...
Nearly a third of FDA medical device adverse events reported late: study
Reports on medical device adverse events widely exceed FDA deadlines, according to a recent study published in the BMJ. Read ...
MedTech Dive3d
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 ...
Medtronic recalls aneurysm-treating device linked to four deaths
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
Modern Healthcare3d
FDA deems Medtronic’s Pipeline Vantage recall ‘most serious’
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
Minn. Police Test Devices to Catch Drug-Impaired Drivers. How'd They Do?
Minnesota law enforcement officers tried out two devices that can detect six classes of drugs and chemicals that can impair ...
Seeking Alpha6d
Nearly a third of FDA medical device adverse events reported late: study
Nearly a third of medical device adverse events were not submitted to the FDA within a 30-day regulatory window, with most late reports filed more than six months after manufacturer notifications ...
Reuters4d
FDA classifies recall of Medtronic embolization devices as 'most serious'
March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified ... reported injuries associated with the use of devices known as Pipeline Vantage Embolization devices.