FDA Device recall Z-0566-2014
Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System
- FDA Device
- Class II
- terminated
- Published 2014-01-01
On 2014-01-01 the FDA classified a Class II recall of Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System by Ziehm Imaging, citing engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the de….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0566-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-21 |
| Published | 2014-01-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ziehm Imaging |
| Distribution | US |
Product
Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Reason
Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
Identifiers
| code_info | 90842 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0566-2014%22
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