FDAMarch 17, 2025device

Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080

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

The hazard

Device may have a small breach in the proximal end of the shaft under the strain relief of the delivery system. Breach is not visibly detectable and may lead to prolonged procedure, blood loss, or air ingress with potential for air embolism.

What to do

FDA enforcement status: Ongoing

Brands named

abbott

UPCs

0081180601156100811806011578

Recall history

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

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