The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.

The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...

The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...

Medtronic (NYSE:MDT) shares snapped seven straight days of losses as the stock closed 0.85% higher, at $88.98 on Thursday. ...

The business, acquired by ICU Medical in 2022, has been dealing with a series of recalls and quality issues over the past ...

The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.

Bausch + Lomb has reported a “voluntary recall” of certain intraocular lenses (IOLs) on its enVista platform due to complications.

The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.

Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients.

BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...

The recall, which instructs customers and distributors ... On March 7, Smiths said it issued an urgent medical device correction to notify customers of a possible problem with the 2.0, 2.5 ...