Inpeco recalls specific FlexLab interface modules that may cause sample cross contamination if the carousel lid stays open or manual processing takes too long. Affected units include part numbers FLX-208-00 and FLX-208-10 with serial numbers listed.
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 is recalling certain FlexLab interface modules that could cause cross contamination of samples if the carousel lid remains open or manual processing takes too long. This affects laboratory equipment used for sample handling in medical testing facilities.
If the sample carousel lid stays open or manual processing takes longer than the module's timeout period, errors can occur leading to cross contamination of samples. This could affect test accuracy and patient results.
Laboratory users with the recalled FlexLab interface modules (part numbers FLX-208-00 and FLX-208-10) are most at risk. These modules are used in medical testing equipment for sample processing.
Check for part numbers FLX-208-00 or FLX-208-10 on the interface module. Affected units have serial numbers listed in the recall notice including AML.001 and FLX.0104 through FLX.103.
Look for serial numbers starting with AML.001 or FLX.0104 through FLX.103 on the interface module.
Reach out to Inpeco S.A. for guidance on next steps if you have the recalled module.
If the sample carousel lid remains open or manual processing takes too long, the module may cause cross contamination of samples, leading to inaccurate test results.
Check for part numbers FLX-208-00 or FLX-208-10 and serial numbers listed in the recall, such as AML.001 or FLX.0104 through FLX.103.
No, but you should check the serial number and contact Inpeco if you have the recalled module to get guidance.
We’ve drafted a message you can send Inpeco to request your refund or repair — edit it as you like.
Subject: Recall Z-2003-2020 — Inpeco Inpeco Hello, I own a Inpeco that is covered by recall Z-2003-2020 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.
