Drug recall
Xoran MiniCAT CT Scanner ID ENT00001
FDA recall event 66344 · Class II · Xoran Technologies, Inc.
Key facts
| Event ID | 66344 |
|---|---|
| Recall numbers | Z-0041-2014 |
| Recalling firm | Xoran Technologies, Inc. |
| Product type | Devices |
| Products | Xoran MiniCAT CT Scanner ID ENT00001 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate. |
| Initiation date | Dec 14, 2009 |
| Report date | Nov 6, 2013 |
| Termination date | Sep 11, 2014 |
| City | Ann Arbor |
| State | MI |
| Country | United States |
| FEI number | 3004198450 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: