Device recall
Z-2311-2008: Stryker Biotech OP- 1 Implant is indicated for use as an alternative to…
FDA device recall · Class III · Stryker Biotech
Key facts
| Recall number (Z-number) | Z-2311-2008 |
|---|---|
| Recall event | 48737 |
| Product | Stryker Biotech OP- 1 Implant is indicated for use as an alternative to autograft in recalcitrant long bone nonunions where use of autograft is unfeasible and alternative treatments have failed. Catalog Number: 100-25 |
| Product code | MPW |
| Recalling firm | Stryker Biotech |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 16, 2008 |
| FEI number | 1000513212 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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