Class II — Xoran Technologies, Inc.
| Recalling firm | Xoran Technologies LLC |
|---|---|
| Registered facility | Xoran Technologies, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate. |
| Product | Xoran MiniCAT CT Scanner ID ENT00001 |
| Quantity | 320 |
| Distribution | Worldwide Distribution - US nationwide |
| Initiated | 2009-12-14 |
| Classified | 2013-10-25 |
| Terminated | 2014-09-11 |
| Recall number | Z-0041-2014 |
| 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, Inc. (Z-0041-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66344/
Alerts for Xoran Technologies LLC
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.