Device recall
Z-2863-2011: Trauma Stryker Medical Stretchers Model 1037 Intended to transport patients in a…
FDA device recall · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2863-2011 |
|---|---|
| Recall event | 59201 |
| Product | Trauma Stryker Medical Stretchers Model 1037 Intended to transport patients in a horizontal position. |
| Product code | FPO |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2013 |
| FEI number | 1831750 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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