Contemporary embolization strategies for active sac management during EVAR.

Medtronic's recall of embolization device has been classified most serious by the U.S. Food and Drug Administration (USFDA), ...

Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of ...

The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage ...

Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...

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

Terumo Neuro, a global leader in neurovascular innovation and a wholly owned subsidiary of Terumo Corporation, proudly marks ...

The U.S. FDA has posted several class I recalls in recent days, including a removal of one model of the Medtronic Vascular’s ...

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

Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...