Beckman Coulter recalls DxI 9000 Access Immunoassay Analyzers with catalog number C11137 due to ground screw issues causing electric shorts, smoke, and delayed patient results.
Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.
Beckman Coulter is recalling DxI 9000 Access Immunoassay Analyzers with specific serial numbers because ground screws on the PCB boards can cause electric shorts. This may lead to smoke, equipment damage, and delayed patient results.
Ground screws on the device's PCB boards can cause electric shorts. This may lead to smoke, equipment damage, and delayed patient results if the device is used without proper maintenance.
Healthcare facilities using the recalled DxI 9000 Access Immunoassay Analyzers with serial numbers 300116-300156 are most at risk. These devices are used for medical testing in labs.
Check for the catalog number C11137 on the DxI 9000 Access Immunoassay Analyzer. The affected units have serial numbers starting with 300116 through 300156.
Look for the serial numbers 300116 through 300156 on the device to confirm if it is affected.
Reach out to Beckman Coulter for further instructions on how to address the issue.
The recalled device is the DxI 9000 Access Immunoassay Analyzer with catalog number C11137.
The affected units have serial numbers starting with 300116 through 300156.
Electric shorts can cause smoke, equipment damage, and delayed patient results.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1529-2025 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1529-2025 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.
