FDADecember 14, 2020device

VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040 /Venovo 9F 14/40/1200mm OUS; VENEL14060 /Venovo 9F 14/60/1200mm OUS; VENEL14080 /Venovo 9F 14/80/1200mm OUS; VENEL14100 /Venovo 9F 14/100/1200mm OUS; VENEL14120 /Venovo 9F 14/120/1200mm OUS; VENEL14140 /Venovo 9F 14/140/...

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

The hazard

Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.

What to do

FDA enforcement status: Ongoing

Brands named

bard peripheral vascularbardbard peripheral

UPCs

008017411022950080174110230100801741102318008017411023250080174110233200801741102349008017411023560080174110222600801741102233008017411022400080174110225700801741102264

Recall history

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

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