FDASeptember 12, 2024device

Abbott Alinity m STI AMP Kit, used with the Alinity m System, product codes: a) REF 09N17-095; b) REF 09N17-090; c) REF 09N17-091;

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

The hazard

Abbott has identified an increase of incidences regarding Error Code (EC) 9198 (Positive control is non-reactive) while using the Alinity m HR HPV AMP Kit and Alinity m STI AMP Kit. Certain invalidated positive assay controls can be traced to iron leaching into the Alinity m Lysis Solution from the lysis transfer pump in the Alinity m System.

What to do

FDA enforcement status: Ongoing

Brands named

abbott molecularabbott

UPCs

008849990485910088499904794500884999049277

Recall history

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

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Abbott Alinity m STI AMP Kit, used with the Alinity m System, product codes: a) REF 09N17-095; b) REF 09N17-090; c) REF 09N17-091; — Recall Details · AllClear