FDAApril 5, 2023device

UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine analysis

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

The hazard

Beckman Coulter has become aware of an intermittent issue in which the optional flag "Previous Sample Had Sperm" was enabled but not displayed so that a carryover event could have been investigated.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

15099590735982

Recall history

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

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