Device recall
Z-2292-2016: Avenir Mller Stem 4 Standard Avenir Mller Stem 6 Lateral Hip joint…
FDA device recall · Class II · Zimmer Gmbh
Key facts
| Recall number (Z-number) | Z-2292-2016 |
|---|---|
| Recall event | 74693 |
| Product | Avenir Mller Stem 4 Standard Avenir Mller Stem 6 Lateral Hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis Intended Use: " Advanced wear of the joint due to degenerative, post-traumatic or rheumatic diseases. " Failed previous hip surgery including joint… |
| Product code | LZO |
| Recalling firm | Zimmer Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2017 |
| 510(k) numbers | K123392 |
| 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