FDANovember 10, 2021device

PIVO Blood Collection Device 20G, REF: 202-0005

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

The hazard

Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects range from no clinical effect up to bloodstream infection.

What to do

FDA enforcement status: Terminated

Brands named

velano vascularvelano

UPCs

00850984007027

Recall history

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

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