Device recall
Z-1217-2013: MyRay RXDC dental unit x-ray unit
FDA device recall · Class II · CEFLA DENTAL GROUP
Key facts
| Recall number (Z-number) | Z-1217-2013 |
|---|---|
| Recall event | 65036 |
| Product | MyRay RXDC dental unit x-ray unit |
| Product code | EHD |
| Recalling firm | CEFLA DENTAL GROUP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 4, 2015 |
| FEI number | 3006610845 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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