FDA Device recall Z-1893-2017
Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
- FDA Device
- Class II
- terminated
- Published 2017-05-24
On 2017-05-24 the FDA classified a Class II recall of Ziehm Imaging solo FD Mobile Fluoroscopic C-arm by Ziehm Imaging, citing during Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified compon….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1893-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-23 |
| Published | 2017-05-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ziehm Imaging |
| Distribution | CA, FL |
Product
Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
Reason
During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component
Identifiers
| code_info | S/N 52199, 52108 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1893-2017%22
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