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

Recall Z-0578-2025 — Ziehm Vision RFD. Interventional fluoroscopic x-ray system

U.S. FDA — Device Enforcement · United States · 2024-08-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0578-2025
Date of alert
2024-08-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Orthoscan, Inc.
Product category
device
Product type
Devices
Reported risk: Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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