FDA issues recall on Medtronic embolization devices

Mar 19, 2025 - 02:56 PM
FDA-device-recall

The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage Embolization Devices due to reports of a higher incidence of the flexible, braided tube part of the device failing to properly attach or stay attached to the blood vessel wall during and after procedures.

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