Device recall
Z-1056-2009: Zimmer Coonrad/Morrey Total Elbow, Interchangeable Ulnar Assembly, plasma…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-1056-2009 |
|---|---|
| Recall event | 50914 |
| Product | Zimmer Coonrad/Morrey Total Elbow, Interchangeable Ulnar Assembly, plasma sprayed, extra small, right, 3 inch length, sterile, Zimmer, Warsaw, IN; REF 32-8105-043-02. The device is utilized for a total elbow arthroplasty surgical procedure. |
| Product code | JDC |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 22, 2009 |
| 510(k) numbers | K053189 |
| 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