Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1889-2020 — Siemens Aptio Automation Centrifuge Module, tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf

U.S. FDA — Device Enforcement · Switzerland · 2020-04-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1889-2020
Date of alert
2020-04-07
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Inpeco S.A.
Product category
device
Product type
Devices
Reported risk: The FlexLab Centrifuge Module loading algorithm may lead to unbalanced loads which could damage the centrifuge.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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