Device recall
Z-1272-02: Portable HDX Intraoral Dental X-Ray. Extraoral Source X-ray System. Part number…
FDA device recall · Class II · Den-Tal-Ez Inc,Star Dental Div
Key facts
| Recall number (Z-number) | Z-1272-02 |
|---|---|
| Recall event | 26413 |
| Product | Portable HDX Intraoral Dental X-Ray. Extraoral Source X-ray System. Part number 300020 |
| Recalling firm | Den-Tal-Ez Inc,Star Dental Div |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 19, 2004 |
| 510(k) numbers | K021378 |
| FEI number | 2520265 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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