Device recall
Z-1311-2010: Pelton & Crane Spirit 3000 Dental Chair. The intended use of this device is for…
FDA device recall · Class III · Pelton & Crane Company
Key facts
| Recall number (Z-number) | Z-1311-2010 |
|---|---|
| Recall event | 54809 |
| Product | Pelton & Crane Spirit 3000 Dental Chair. The intended use of this device is for properly positioning patients to perform dental procedures. |
| Product code | KLC |
| Recalling firm | Pelton & Crane Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 11, 2010 |
| FEI number | 1017522 |
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