FDAFebruary 1, 2024device

In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit, REF 01N15-010; (2) Abbott Vysis LSI D13S319 (13q14.3) SpectrumOrange Probe, REF 01N34-020;

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

The hazard

Products that were intended for export only which were not approved or registered in accordance with U.S. specifications were shipped to U.S. customers.

What to do

FDA enforcement status: Ongoing

Brands named

abbott molecularabbott

UPCs

0088499903536200884999000766

Recall history

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

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