Device recall
Z-0651-2016: Vantage Panoramic X-Ray System used to perform dental and orthodontic…
FDA device recall · Class II · Midmark Corp dba Progeny Inc
Key facts
| Recall number (Z-number) | Z-0651-2016 |
|---|---|
| Recall event | 70765 |
| Product | 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 examination and diagnosis of diseases of the teeth, jaw and oral structures. When the system is… |
| Product code | MUH |
| Recalling firm | Midmark Corp dba Progeny Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 29, 2017 |
| 510(k) numbers | K122643 |
| FEI number | 3000210017 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database