The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage ...
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
Monogram Technologies secured 510(k) clearance for its robotic knee replacement system, while Vicarious Surgical blamed ...
Medtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
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FOX 13 Tampa Bay on MSN6 popular acne treatment products recalled for elevated levels of benzeneThe FDA has recalled six popular acne treatment products due to elevated levels of benzene. Experts say that some exposure to ...
Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
In a notice posted to the agency’s website, the FDA noted that on January 30, 2025, Medtronic (MDT) Neurovascular sent all affected customers ...
The FDA announced that Medtronic initiated a device recall and correction for embolization devices. The FDA has identified ...
BD, Medtronic and Abbott were among the top 10 medical device manufacturers with the highest number of late reports, the ...
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