Data Foundry

Medical device recalls 2026

Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software… — Class II medical device recall Z-2974-2026

Ongoing recall by Beckman Coulter Inc., reported 2026-08-26, distributed nationwide. a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test r

Recall numberZ-2974-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBeckman Coulter Inc., Brea, CA, United States
Recall initiated2026-07-15
Classified2026-08-17
Reported by FDA2026-08-26
DistributedNationwide (US)
Reason classessoftware
UPC / GTIN / UDI-DI14987666545058, 14987666545065
Model numbersC63519, C63520

Product

Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or lower: 1) AU w/out ISE, Part Number C63519; 2) AU w/ISE, Part Number C63520; DxC 500 AU Clinical Chemistry Analyzers

Reason for recall

a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2974-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.