Device recall
Z-1727-2011: Stryker Biotech OP-1 Putty (OP-1, BMP-7, bone morphogenetic protein) "Catalog…
FDA device recall · Class II · Stryker Biotech
Key facts
| Recall number (Z-number) | Z-1727-2011 |
|---|---|
| Recall event | 56962 |
| Product | Stryker Biotech OP-1 Putty (OP-1, BMP-7, bone morphogenetic protein) "Catalog numbers: 300-50, 300-55 OP-1 Putty is authorized by Federal law for use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous… |
| Product code | OJZ |
| Recalling firm | Stryker Biotech |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 20, 2012 |
| 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