Beckman Coulter recalls DxI 9000 Access Immunoassay Analyzers with misaligned encoder wheels that may cause instrument stoppages and delays in patient results.
the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.
Beckman Coulter is recalling DxI 9000 Access Immunoassay Analyzers due to a misaligned encoder wheel that can cause the instrument to stop unexpectedly. This poses a risk of delayed patient results, which could impact healthcare workflows.
The encoder wheel on the motor shaft is misaligned, causing increased slippage errors. This leads to the instrument stopping unexpectedly, which may delay patient results and disrupt healthcare workflows.
Healthcare facilities using the DxI 9000 Access Immunoassay Analyzer with the specified serial numbers are most at risk. Patients and staff relying on timely lab results could be affected.
Check the serial numbers listed in the recall notice: 300116-300117, 300123-300124, and other ranges up to 300352. The product is sold under the catalog number C11137.
Verify your DxI 9000 Access Immunoassay Analyzer's serial number against the list provided in the recall notice.
The DxI 9000 encoder wheel was misaligned on the motor shaft, causing increased slippage errors and potential instrument stoppages.
The instrument may stop unexpectedly, leading to delays in patient results which could impact healthcare workflows.
Check the serial number against the list: 300116-300117, 300123-300124, and other ranges up to 300352.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1388-2025 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1388-2025 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.
