Beckman Coulter recalls REMISOL Advance software version 2.5 with UDI-DI code 15099590802073 due to incorrect combo test results. Affected users should check their software version and contact for remedy.
Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes.
Beckman Coulter is recalling REMISOL Advance data management software version 2.5 with UDI-DI code 15099590802073 because it may replace final combo test results with sub-results, causing incorrect reporting. This could lead to wrong test outcomes if the software is used without correction.
The software may replace the final combo test result with one of the sub-results, leading to incorrect reporting of test outcomes. This happens due to software issues that affect how the system handles combined assay results.
Users of REMISOL Advance data management software version 2.5 with UDI-DI code 15099590802073 are affected. Laboratory staff and healthcare professionals using this software for test management are most at risk of incorrect results.
Check for software version 2.5 on REMISOL Advance with UDI-DI code 15099590802073. The product includes the Normand Info REMISOL Advance Data Manager for 128 connections.
Verify your REMISOL Advance software version is 2.5 with UDI-DI code 15099590802073.
Software version 2.5 with UDI-DI code 15099590802073.
The software may replace the final combo test result with one of the sub-results, causing incorrect reporting of test outcomes.
Check your software version and contact Beckman Coulter for remedy options.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-2834-2026 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-2834-2026 from Beckman Coulter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
