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

Recall Z-0587-2017 — FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation.

U.S. FDA — Device Enforcement · Switzerland · 2016-10-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0587-2017
Date of alert
2016-10-04
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Inpeco S.A.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
693822160
Reported risk: Inpeco received several notifications from the field about burnt schuko sockets. The customers reported that some smoke was seen coming from the damaged sockets.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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