Device recall
Z-0644-2019: Avenir Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number…
FDA device recall · Class II · Zimmer GmbH
Key facts
| Recall number (Z-number) | Z-0644-2019 |
|---|---|
| Recall event | 81608 |
| Product | Avenir Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number: 01.06010.001 - Product Usage: Avenir@ Muller Stems are intended to reduce pain and increase hip mobility through long term cementless fixation of total or hemi hip arthroplasty in the femur of patients with an adequate bone… |
| Product code | LZO |
| Recalling firm | Zimmer GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2020 |
| 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