Beckman Coulter recalls DxI 9000 Access Immunoassay Analyzers with specific serial numbers due to potential wash wheel mixer malfunction causing test delays and system errors.
The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash Wheel Dispense Arm Spin Mixer Error that is displayed on the navigation bar in the User Interface. The analyzer enters the red system status and will generate a SYS flag. The tests that are in progress may be cancelled and may cause a delay in reporting patient results
Beckman Coulter is recalling certain DxI 9000 Access Immunoassay Analyzers because their wash wheel mixer may not spin freely, which can cause tests to cancel and delay patient results. This issue affects laboratory equipment used for medical testing.
The wash wheel mixer may not spin freely within the idler pulley housing, causing the analyzer to generate a 'Wash Wheel Dispense Arm Spin Mixer Error' message. This can cancel ongoing tests and delay patient results without causing physical harm.
Laboratories using the recalled DxI 9000 Access Immunoassay Analyzers with specific serial numbers are most at risk. Patients may experience delayed test results if the analyzer is in use.
Check for the catalog number C11137 and serial numbers listed in the recall notice (e.g., 300116, 300117, etc.). The device is used in laboratories for medical testing.
Look for a 'Wash Wheel Dispense Arm Spin Mixer Error' message on the analyzer's navigation bar.
Confirm the device has a serial number from the list provided in the recall notice.
The specific model is the DxI 9000 Access Immunoassay Analyzer with catalog number C11137.
The issue can cancel ongoing tests and delay patient results, but does not cause physical injury.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1326-2025 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1326-2025 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.
