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

Recall Z-2007-2012 — Monaco Product Usage: Planning of radiation therapy

U.S. FDA — Device Enforcement · United States · 2012-06-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2007-2012
Date of alert
2012-06-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Elekta, Inc.
Product category
device
Product type
Devices
Reported risk: Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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