Drug recall
DeGotzen XRay unit XGenus Dental X-ray unit.
FDA recall event 64734 · Class II · DeGotzen
Key facts
| Event ID | 64734 |
|---|---|
| Recall numbers | Z-1020-2013 |
| Recalling firm | DeGotzen |
| Product type | Devices |
| Products | DeGotzen XRay unit XGenus Dental X-ray unit. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | It was discovered at the WEAC Labs method sample did not meet requirements for labeling and certification |
| Initiation date | Sep 26, 2012 |
| Report date | Apr 24, 2013 |
| Termination date | May 7, 2018 |
| City | Olgiate Olona Varese |
| Country | Italy |
| FEI number | 3009685455 |
At a glance
- 1–9 Products in this recall
- None 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: