Device recall
Z-0467-03: Restoration #8 HA Hip Stem, Catalog No. 6013-1216 and Restoration #8 HA Hip…
FDA device recall · Class III · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-0467-03 |
|---|---|
| Recall event | 25321 |
| Product | Restoration #8 HA Hip Stem, Catalog No. 6013-1216 and Restoration #8 HA Hip Stem, Catalog No. 6013-1218. |
| Product code | MEH |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 1, 2003 |
| 510(k) numbers | K944836 |
| FEI number | 3003070421 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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