Device recall
Z-0576-2011: Zimmer Trabecular Metal Reverse Shoulder System Surgical Technique. Catalog…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0576-2011 |
|---|---|
| Recall event | 56731 |
| Product | Zimmer Trabecular Metal Reverse Shoulder System Surgical Technique. Catalog Number 97-4309-003-00, Rev. 4. The Zimmer Trabecular Metal Reverse Shoulder System is a treatment option for patients with severe rotator cuff (RC) deficiency. The stem was designed so that its bearing surfaces, as compared… |
| Product code | KWT |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2012 |
| 510(k) numbers | K041549, K050761, K052906, K060704 |
| FEI number | 1000220733 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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