FDA Device recall Z-0041-2014
Xoran MiniCAT CT Scanner ID ENT00001
- FDA Device
- Class II
- terminated
- Published 2013-11-06
On 2013-11-06 the FDA classified a Class II recall of Xoran MiniCAT CT Scanner ID ENT00001 by Xoran Technologies, citing failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0041-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2009-12-14 |
| Published | 2013-11-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Xoran Technologies |
| Distribution | US |
Product
Xoran MiniCAT CT Scanner ID ENT00001
Reason
Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.
Identifiers
| code_info | minicat |
|---|
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-0041-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.