Device recall
Z-2228-2008: Metal Hemiarthroplasty, MDL E536687, Part # 03-6000-1, 03-6000-02, 03-600-03…
FDA device recall · Class II · OrthoPro LLC
Key facts
| Recall number (Z-number) | Z-2228-2008 |
|---|---|
| Recall event | 48693 |
| Product | Metal Hemiarthroplasty, MDL E536687, Part # 03-6000-1, 03-6000-02, 03-600-03, 03-6000-04, OrthoPro LLC, Salt Lake City, UT Hemi is designed to supplement first metatarsal Phalangeal joint arthroplasty. |
| Product code | KWD |
| Recalling firm | OrthoPro LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 24, 2008 |
| 510(k) numbers | K071243 |
| FEI number | 3005252592 |
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