Abbott recalls Accelerator APS Aliquoter Module (List 07L40) due to potential sample dilution from AQM clot detection errors, which could cause incorrect lab results. Affected units include all field serial numbers.
In the case of an AQM clot detection error a portion of the distilled water from the Aliquoter Module hydraulic circuit may be dispensed into the Primary Tube leading to sample dilution, which could lead to incorrect results.
Abbott is recalling its Accelerator APS Aliquot:er Module (List 07L40) because a technical error might dilute lab samples, leading to incorrect test results. This affects clinical lab equipment used for sample processing.
When the AQM clot detection system detects an error, a small amount of distilled water from the Aliquoter Module's hydraulic circuit may be accidentally dispensed into the sample tube. This dilutes the sample, potentially causing inaccurate lab results.
Clinical laboratory users who operate the Accelerator APS Workcell system are most affected. The recall applies to all units sold in the field with serial numbers in the affected list.
Check if your Accelerator APS Aliquoter Module has a serial number listed in the field (all units are affected). The product is used in clinical laboratories for sample processing.
Verify your module's serial number against the affected list provided by Abbott.
The recall is due to a potential AQM clot detection error that could cause distilled water to be dispensed into the sample tube, leading to sample dilution and incorrect lab results.
All field serial numbers are affected; check your module's serial number against the list provided by Abbott.
The recall does not specify a remedy, so contact Abbott directly for guidance on next steps.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-2251-2020 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-2251-2020 from Abbott. 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.
