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

Recall Z-1726-2020 — Canon Aquilion One, Model TSX-305A/3 V8.3 with FIRST 2.1

U.S. FDA — Device Enforcement · United States · 2019-03-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1726-2020
Date of alert
2019-03-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Canon Medical System, USA, INC.
Product category
device
Product type
Devices
Reported risk: Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off and reboot. Loss of the acquired raw data would occur.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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