RecallRadar

FDA Device recall Z-0576-2025

Ziehm Vision FD. Interventional fluoroscopic x-ray system

On 2024-12-11 the FDA classified a Class II recall of Ziehm Vision FD. Interventional fluoroscopic x-ray system by Orthoscan, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0576-2025
ClassificationClass II
Statusongoing
Initiated2024-08-08
Published2024-12-11
Last updated2026-09-13 11:57 UTC
CompanyOrthoscan
DistributionPR

Product

Ziehm Vision FD. Interventional fluoroscopic x-ray system

Reason

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.

Identifiers

code_info
UDI: EZIEZIEHMVISIONFD1651 Serial Numbers: 93412, 93443, 93451, 93452, 93461, 93483, 93485, 93486, 93503, 93619, 93620…UDI: EZIEZIEHMVISIONFD1651 Serial Numbers: 93412, 93443, 93451, 93452, 93461, 93483, 93485, 93486, 93503, 93619, 93620, 93621. 93622 93623 93628 93629 93660 93661 93662 93626 93625 93627

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0576-2025%22

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