FDAMarch 29, 2016device

ev3, PowerCross" 0.018" OTW PTA Dilatation Catheter, model: AB18W030200150, Sterile EO, Rx Only.

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

The hazard

Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots of the PowerCross 0.018" ¿ Over the Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter because the product is mislabeled.

What to do

FDA enforcement status: Terminated

Brands named

ev3

Recall history

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

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