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BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD. recalls DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.
Recalled March 5, 2025 · FDA recall Z-1233-2025 · BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU)
Hazard
Beckman Coulter has identified an issue which prevents the DxC 500 AU instrument from providing the correct onboard stability (Open Expiration) dates for assays that were loaded prior to a software upgrade (e.g. 1.3 to 1.4, 1.4 to 1.4.1, etc.). As a result, assays that have expired may still be used for sample processing, leading to inaccurate or erroneous patient test results. The issue only happens on assays loaded before instruments doing upgrades and does not impact new installation. It does not impact the assays loaded after upgrade. · FDA Class II
Units
56
Sold at
US: MA, CA, SC, LA, OK, GA, AL, TX, OR, ID, CO, MN, NY, MS, PA, WA, IL, MI, PR. OUS: Lebanon, Poland, Ghana, Spain, South Africa, Slovakia, Ghana, Croatia, Seychelles, Australia, Republic of Korea
Description
Beckman Coulter has identified an issue which prevents the DxC 500 AU instrument from providing the correct onboard stability (Open Expiration) dates for assays that were loaded prior to a software upgrade (e.g. 1.3 to 1.4, 1.4 to 1.4.1, etc.). As a result, assays that have expired may still be used for sample processing, leading to inaccurate or erroneous patient test results. The issue only happens on assays loaded before instruments doing upgrades and does not impact new installation. It does not impact the assays loaded after upgrade.
Product
DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.
Manufacturer(s)
BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.
Made in
China
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →