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
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 ...
Medtronic ventilators helped save lives during the pandemic, so why is the company shutting down the business?
Medtronic’s top ventilator executive began fielding pleas from world leaders' representatives five years ago, as pressure ...
US health agencies announce plan to strengthen domestic infant formula supply
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 ...
MedPage Today on MSN6d
FDA's Deadline Ignored in Nearly 30% of Device Safety Reports
Nearly 10% of postmarket device safety reports in MAUDE were submitted over 6 months after the safety event occurred.
Medical Device Network on MSN5d
Nearly a third of FDA medical device adverse event reports filed late
A study has found that nearly a third of medical device AEs were reported by manufacturers later than FDA's required 30-day ...
Abbott's Narrow Economic Moat Rests on a Solid Product Portfolio
In most cases, Abbott is one of three or four competitors that dominate the market, including nutrition, cardiac rhythm management devices, surgical heart valves, continuous glucose monitors, coronary ...
Healio12d
Q&A: New technology may become second mechanical heart pump available in US
Left ventricular assist devices, which are mechanical heart pumps, are an important treatment for patients with advanced ...