FDAJune 11, 2017device

Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900, Product Catalog No. 022930. Product Usage: The AIA-900 Automated Enzyme Immunoassay System is an automated analyzer for in vitro diagnostic use that measures a variety of substances in serum, plasma, and or urine using the AIA-PACK reagent series.

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

The hazard

This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential malfunction has been attributed to aging and premature deterioration of the Pl collector current.

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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