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

Recall Z-2477-2019 — Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Numbers : 05964075001 cobas c 701 module part Numbers : 05641489001 cobas c 702 module part Numbers : 06473245001

U.S. FDA — Device Enforcement · United States · 2019-07-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2477-2019
Date of alert
2019-07-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Roche Diagnostics Operations, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05964075001
Reported risk: Quality issue with high pressure solenoid valves
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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