Drug recall
Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage…
FDA recall event 70765 · Class II · Midmark Corp dba Progeny Inc
Key facts
| Event ID | 70765 |
|---|---|
| Recall numbers | Z-0651-2016 |
| Recalling firm | Midmark Corp dba Progeny Inc |
| Product type | Devices |
| Products | Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray System is a class II extra oral X-Ray system used to provide dental radiographic… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failure of the primary collimator may result in unintentional movement of the device. The unintentional movement will not result in the generation of an error message. |
| Initiation date | Sep 4, 2014 |
| Report date | Feb 3, 2016 |
| Termination date | Dec 29, 2017 |
| City | Lincolnshire |
| State | IL |
| Country | United States |
| FEI number | 3000210017 |
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: