Lower riskMedical device recall · FDA · Published June 4, 2024
Beckman Coulter Dxl 9000 Analyzer Recall: Nonconforming USB Cables May Cause Delayed
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.
Take action
Contact the company
📍Recalling firmBeckman Coulter, Inc.1000 Lake Hazeltine Dr · Chaska, MN 55318-1037
“Beckman Coulter Dxl 9000 Analyzer Recall: Nonconforming USB Cables May Cause Delayed.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54929-beckman-coulter-dxl-9000-analyzer-recall-nonconforming-usb-cables-may. Based on FDA recall #Z-2414-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2414-2024%22&limit=1).
The FDA announced on June 4, 2024, that Beckman Coulter, Inc. is recalling its Dxl 9000 Access Immunoassay Analyzer due to nonconforming USB cables with brass contacts that may corrode and delay patient results. The agency issued the recall for the Class II device.
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.
Context
GovInfoNow's records show Beckman Coulter, Inc. has 132 other recalls on record since June 20, 2017. Other recent recalls include the Beckman Coulter DxC 500 AU Modules with Software 1.5 (July 15, 2026), the MicroScan LabPro V5.03 Panel Update 11 (June 26, 2026), and the Access Total T4 Calibrator Recall (March 16, 2026). Other recent recalls of similar products include the Beckman Coulter DxC 700 AU Recall (Jan. 30, 2026), the Beckman Coulter AU5800 Chemistry Analyzer Recall (Jan. 30, 2026), and the AU480 Chemistry Analyzer recall (Aug. 3, 2026).
How to tell if you have this one
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.
Brand
Beckman Coulter
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Look for the serial numbers listed in the recall notice (e.g., 300117, 300116, etc.) on your Dxl 9000 Access Immunoassay Analyzer.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 6 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of FL, IN, KS, NH, PA, and TX. The countries of Australia, Austria, Belgium, Brazil, Croatia, Czechia, Egypt, France, Germany, Hungary, Ireland, Israel, Italy, Netherlands, New Zealand,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Indiana, Kansas, New Hampshire, Pennsylvania, Texas.
Recall timeline
FDA published this recall 57 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2414-2024 (June 4, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2414-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.