FDAOctober 21, 2016device

is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM autoantibodies specific for the phospholipid cardiolipin in human serum and EDTA, lithium heparin or citrated plasma. It is intended to assess of anti-cardiolipin IgG autoantibody levels in pa...

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

The hazard

Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

What to do

FDA enforcement status: Terminated

Brands named

euro diagnostica abeuroeuro diagnostica

Recall history

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

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