Xoran MiniCAT CT Scanner ID ENT00001 — Class II medical device recall Z-0041-2014
Terminated recall by Xoran Technologies, Inc., reported 2013-11-06, distributed nationwide. Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rot
| Recall number | Z-0041-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Xoran Technologies, Inc., Ann Arbor, MI, United States |
| Recall initiated | 2009-12-14 |
| Classified | 2013-10-25 |
| Reported by FDA | 2013-11-06 |
| Terminated | 2014-09-11 |
| Distributed | Nationwide (US) |
| Quantity | 320 |
Product
Xoran MiniCAT CT Scanner ID ENT00001
Reason for recall
Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.
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-0041-2014. 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.