Inpeco recalls specific Abbott Accelerator a3600 interface modules (serial numbers ACP.001-ACP.442) due to potential cross contamination if sample carousel lid remains open or manual processing takes too long.
When analyzer sample carousel lid remains open or manual process is too long, Module timeout expiry errors could occur causing cross contamination of samples.
Inpeco has recalled specific Abbott Accelerator a3600 interface modules (serial numbers ACP.001 to ACP.442) because leaving the sample carousel lid open or taking too long with manual processing can cause cross contamination of samples. This affects laboratory equipment used for sample processing.
If the sample carousel lid stays open or manual processing takes too long, the interface module may time out, causing cross contamination between samples. This could lead to inaccurate test results but does not cause physical harm.
Laboratories using the Abbott Accelerator a3600 system with the recalled interface modules (serial numbers ACP.001 to ACP.442) are most at risk. These modules are part of the FlexLab system for automated sample processing.
Check if your Abbott Accelerator a3600 interface module has serial numbers starting with ACP.001 through ACP.442. The product is part of the FlexLab system for laboratory sample processing.
Identify if your interface module has a serial number in the range ACP.001 to ACP.442.
The recalled product is the Abbott Accelerator a3600 interface module with serial numbers ACP.001 to ACP.442.
If the sample carousel lid remains open or manual processing takes too long, cross contamination of samples may occur, leading to inaccurate test results.
No, the recall does not require immediate discontinuation. Affected users should check their serial numbers and follow the provided action steps.
We’ve drafted a message you can send Inpeco to request your refund or repair — edit it as you like.
Subject: Recall Z-2004-2020 — Inpeco Inpeco Hello, I own a Inpeco that is covered by recall Z-2004-2020 from Inpeco. 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.
