Beckman Coulter recalls Dxl 9000 Access Immunoassay Analyzers with nonconforming USB cables that may corrode over time, causing delayed patient results. Affected units have specific serial numbers and catalog numbers.
The analyzers were built with nonconforming USB cables made with brass contacts instead of specified gold contacts. Brass contacts may corrode over time, leading to loss of internal instrument communication and delayed patient results.
Beckman Coulter is recalling Dxl 9000 Access Immunoassay Analyzers that came with nonconforming USB cables using brass contacts instead of gold. This could lead to communication issues and delayed patient results over time.
The USB cables in these analyzers use brass contacts instead of the specified gold contacts. Over time, brass can corrode, which may cause the instrument to lose communication with its internal systems and delay patient test results.
Healthcare facilities that use the Dxl 9000 Access Immunoassay Analyzer for patient testing are most likely affected. The risk is low as the issue involves potential communication delays rather than immediate safety hazards.
Check for the catalog number C11137 and serial numbers listed in the recall notice. The affected units have specific serial numbers starting with 3001 and ending with various numbers.
Look for the serial numbers listed in the recall notice (e.g., 300117, 300116, etc.) on your Dxl 9000 Access Immunoassay Analyzer.
The analyzers were built with nonconforming USB cables made with brass contacts instead of specified gold contacts, which may corrode over time and cause communication issues.
Check if your Dxl 9000 Access Immunoassay Analyzer has the catalog number C11137 and one of the specific serial numbers listed in the recall notice.
The recall notice does not specify a remedy, so affected users should check with the manufacturer for further instructions.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-2414-2024 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-2414-2024 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.
