Device recall
Z-2144-2009: Corin Unipolar Adapter Sleeve, For use with Corin Unipolar CoCr Heads; Not for…
FDA device recall · Class III · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-2144-2009 |
|---|---|
| Recall event | 52713 |
| Product | Corin Unipolar Adapter Sleeve, For use with Corin Unipolar CoCr Heads; Not for use w/ceramic heads; not for use w/ Stainless Steel implants. Stryker Orthopaedics. Indicated for use in partial hip replacement procedures for patients suffering from pain and disability due to a variety of related bone… |
| Product code | KWL |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2010 |
| 510(k) numbers | K071471 |
| FEI number | 3003070421 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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