Device recall
Z-0315-2011: Distal Centralizer 10 mm
FDA device recall · Class II · Ortho Development Corporation
Key facts
| Recall number (Z-number) | Z-0315-2011 |
|---|---|
| Recall event | 56499 |
| Product | Distal Centralizer 10 mm |
| Product code | KWY |
| Recalling firm | Ortho Development Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2010 |
| 510(k) numbers | K962448 |
| FEI number | 3017298928 |
At a glance
- 1–9 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