Device recall
Z-0999-2013: CareStream Dental CS 2100 X-ray system Product Usage: The expected usage…
FDA device recall · Class II · Trophy Sas
Key facts
| Recall number (Z-number) | Z-0999-2013 |
|---|---|
| Recall event | 64589 |
| Product | CareStream Dental CS 2100 X-ray system Product Usage: The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures. |
| Product code | EAP |
| Recalling firm | Trophy Sas |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2017 |
| FEI number | 7695 |
At a glance
- None 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