FDAOctober 30, 2025device

Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10

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

The hazard

Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.

What to do

FDA enforcement status: Ongoing

Brands named

cepheid

UPCs

07332940007102

Recall history

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

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