FDA recall Z-0575-2025

Orthoscan, Inc. · Class II · device

Product

Ziehm Vision system, x-ray, tomography, computed.

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).

Key facts

Status
Ongoing
Initiation date
2024-08-08
Report date
2024-12-11
Voluntary/Mandated
FDA Mandated
Location
Scottsdale, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0575-2025