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FDAJuly 10, 2017device

Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.

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

The hazard

Needle supplier indicated the presence of loose polypropylene foreign matter above release specification.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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