FDANovember 15, 2018device

V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180

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

The hazard

During in-house testing it was determined that their is a possibility that during a sample run, the instrument may aspirate a sample from the wrong sample container resulting in a sample result and patient ID mismatch. If not detected, this may lead to an incorrect patient report.

What to do

FDA enforcement status: Ongoing

Brands named

vital scientific n vvitalvital scientific

UPCs

03661540600180

Recall history

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

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