Class II — Xoran Technologies, LLC
| Recalling firm | Xoran Technologies LLC |
|---|---|
| Registered facility | Xoran Technologies, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose. |
| Product | Xoran MiniCAT X-ray imaging device |
| Quantity | 432 |
| Distribution | Nationwide Distribution |
| Initiated | 2014-09-08 |
| Classified | 2015-03-02 |
| Terminated | 2016-02-02 |
| Recall number | Z-1210-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Xoran Technologies, LLC (Z-1210-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69939/
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