Reported Dec 24, 2025 · Ongoing

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

Cepheid

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cepheid · 904 E Caribbean Dr · Sunnyvale, CA · 94089-1189

Is this the product you have?

  • Brand NameXpert¿
  • BCR-ABL Ultra Model/Catalog NumberGXBCRABL-10
Lot codes and dates
  • UDI007332940001834/Lot
  • Numbers
    • 1001452775
    • 1001457465
    • 1001457622
    • 1001459091
    • 1001462586
    • 1001462625
    • 1001463944
    • 1001465391
    • 1001469480
    • 1001473229
    • 1001474930
    • 1001477474
    • 1001480636
    • 1001483324
    • 1001486594
    • 1001492908
    • 1001493823
    • 1001495811
    • 1001498202
    • 1001501650
Amount recalled
4032 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:56 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.