FDASeptember 28, 2018device

Tosoh AIA-900 immunoassay Analyzer

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

The hazard

A software issue may cause the liquid volume detection entries for 2nd and 3rd reagent bottles to be overwritten with the data from the 1st reagent bottle. Tosoh has released software version 2.51 (or later) to fix the problem. This failure is mitigated by the hardware design. The consequence would be a slight delay in testing patient sample or reporting patient result.

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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