Device recall
Z-0852-03: Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 8mm Lft.
FDA device recall · Class II · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-0852-03 |
|---|---|
| Recall event | 25640 |
| Product | Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 8mm Lft. |
| Product code | JWH |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2004 |
| 510(k) numbers | K973121 |
| 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