Device recall
Z-0575-2011: Zimmer Trabecular Metal Humeral Stem 4-Part Fracture Surgical Technique. Catalog…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0575-2011 |
|---|---|
| Recall event | 56731 |
| Product | Zimmer Trabecular Metal Humeral Stem 4-Part Fracture Surgical Technique. Catalog Number 97-4309-004-00, Rev. 3. The Zimmer Trabecular Metal Shoulder System consists of conventional and reverse, semi- and nonconstrained (resurfacing) shoulder prostheses for total or hemi-arthroplasty applications… |
| 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