FDANovember 30, 2018device

AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of vitamin B12 (B12) in human serum on Tosoh AIA System analyzers.

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

The hazard

Potential for fluorescein interference to cause inaccurately elevated results for certain Tosoh AIA assays

What to do

FDA enforcement status: Terminated

Brands named

tosoh biosciencetosoh

Recall history

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

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