Device recall
Z-0060-2011: Zimmer Trabecular metal Modular Acetabular system 56 mm Porous shell with…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0060-2011 |
|---|---|
| Recall event | 56651 |
| Product | Zimmer Trabecular metal Modular Acetabular system 56 mm Porous shell with cluster holes, Catalog 00-6202-056-22, Zimmer Inc., Warsaw, IN. This device is indicated for primary or revision surgery for rehabilitating hips damaged as the result of noninflammatory degenerative joint disease, including… |
| Product code | LPH |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2011 |
| 510(k) numbers | K021891 |
| FEI number | 1000220733 |
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