Device recall
Z-0624-05: Heraeus Kulzer brand P2 Magnum 360 Heavy 3X (2x360); catalog number 66009585.
FDA device recall · Class III · Heraeus Kulzer Inc.
Key facts
| Recall number (Z-number) | Z-0624-05 |
|---|---|
| Recall event | 29993 |
| Product | Heraeus Kulzer brand P2 Magnum 360 Heavy 3X (2x360); catalog number 66009585. |
| Product code | ELW |
| Recalling firm | Heraeus Kulzer Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 5, 2005 |
| 510(k) numbers | K030318 |
| FEI number | 1821514 |
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