FDAFebruary 4, 2022device

Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The device has similarities in design to another device that the firm recently issued a field correction on due to instances of tip detachment and embolization.

What to do

FDA enforcement status: Terminated

Brands named

ev3

UPCs

00763000402419

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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