Device recall
Z-3014-2011: Metha(R) Hip System Cobalt Chrome (CoCr) Metha Modular Neck Adapters used with…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-3014-2011 |
|---|---|
| Recall event | 59463 |
| Product | Metha(R) Hip System Cobalt Chrome (CoCr) Metha Modular Neck Adapters used with the Metha Modular Short Hip Stems. Aesculap AG. Intended to replace a hip joint |
| Product code | LZO |
| Recalling firm | Aesculap Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 19, 2013 |
| 510(k) numbers | K071916 |
| FEI number | 2916714 |
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