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

Recall Z-1466-2017 — Artis Q and Q.Zen fluoroscopic x-ray system

U.S. FDA — Device Enforcement · United States · 2017-02-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1466-2017
Date of alert
2017-02-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Reported risk: A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids. In rare cases, the introduction of liquids in the wireless foot switch housing could result in the failure of the foot switch.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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