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

Recall Z-0152-2015 — Laksell Gamma Knife Perfexion

U.S. FDA — Device Enforcement · United States · 2014-10-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0152-2015
Date of alert
2014-10-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Elekta, Inc.
Product category
device
Product type
Devices
Reported risk: Elekta has become aware that the latches may be locked before they have been fully turned resulting in a poorly locked frame.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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