Device recall
Z-1295-03: T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S.
FDA device recall · Class III · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-1295-03 |
|---|---|
| Recall event | 26996 |
| Product | T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S. |
| Product code | HSB |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 30, 2003 |
| 510(k) numbers | K003018 |
| 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