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

Recall Z-1090-2017 — cobas p 612 pre-analytical system; Pre-analytical sample handling that includes de-capping, Aliquotting and sorting of samples for analysis.

U.S. FDA — Device Enforcement · United States · 2016-12-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1090-2017
Date of alert
2016-12-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Roche Diagnostics Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
63004316
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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