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

Recall Z-2052-2016 — MOSAIQ Oncology Information System

U.S. FDA — Device Enforcement · United States · 2016-06-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2052-2016
Date of alert
2016-06-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Elekta, Inc.
Product category
device
Product type
Devices
Reported risk: It is possible that that the selected Plan-of-the Day could be accidently changed by scrolling the mouse wheel up and down and inadvertently selecting another plan.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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