BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.
1 federal recall on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-03-05FDA-DeviceClass IIDxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.
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.
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