Device recall
Z-0119-2016: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer Natural…
FDA device recall · Class II · Zimmer Gmbh
Key facts
| Recall number (Z-number) | Z-0119-2016 |
|---|---|
| Recall event | 72123 |
| Product | Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone. |
| Product code | HSB |
| Recalling firm | Zimmer Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 15, 2016 |
| 510(k) numbers | K091566 |
| FEI number | 3005233524 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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