Beckman Coulter recalls MicroScan Neg Multidrug Resistant MIC 1 REF C32368 with UDI-DI code 15099590720568 due to incorrect processing in multidrug resistant testing. This may affect lab results for gram-negative bacteria.
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
Beckman Coulter is recalling a specific multidrug resistant test kit because it may process incorrectly, potentially leading to inaccurate lab results for certain bacteria. This affects healthcare labs using the product for testing gram-negative bacteria.
The test kit may process incorrectly due to a manufacturing issue, which could lead to inaccurate lab results. This might affect the correct identification of bacteria and their antibiotic resistance, potentially impacting treatment decisions.
Healthcare labs that use this test kit for gram-negative bacteria testing. Patients receiving treatment based on inaccurate lab results may be at risk.
Check for the product name 'MicroScan Neg Multidrug Resistant MIC 1 REF C32368' and UDI-DI code 15099590720568. The kit was sold with lot number 2026-05-08.
Verify the product name and UDI-DI code to confirm if you have the recalled item.
The MicroScan Neg Multidrug Resistant MIC 1 REF C32368 with UDI-DI code 15099590720568.
Due to a manufacturing issue that may cause incorrect processing of the multidrug resistant test.
The recall record does not specify a remedy.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1794-2026 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1794-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
