Ziehm Vision — Class II medical device recall Z-0566-2014
Terminated recall by Ziehm Imaging Inc, reported 2014-01-01, distributed nationwide. Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency swi
| Recall number | Z-0566-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ziehm Imaging Inc, Orlando, FL, United States |
| Recall initiated | 2013-11-21 |
| Classified | 2013-12-24 |
| Reported by FDA | 2014-01-01 |
| Terminated | 2014-06-23 |
| Distributed | Nationwide (US) |
| Quantity | 1 devices |
Product
Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0566-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.