Medical Device Recall: Ziehm Vision system, x-ray, tomography, computed.
Orthoscan, Inc. · August 8, 2024
Reason for Recall
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.
Distribution
U.S. (including Puerto Rico).
Quantity Affected
3
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0575-2025
Status: ongoing
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