FDASeptember 15, 2017device

Panther(R) System, Catalog Number 902615, For Use with Hologic Assays, For In Vitro Diagnostic Use

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

The hazard

An incorrect incubator was installed on one Panther System which potentially led to incorrect Aptima Combo 2(R) assay (AC2) results.

What to do

FDA enforcement status: Terminated

Brands named

hologic

UPCs

20900001124

Recall history

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

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