Device recall
Z-0438-2019: The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
FDA device recall · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0438-2019 |
|---|---|
| Recall event | 81211 |
| Product | The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option |
| Product code | FNL |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2020 |
| FEI number | 1831750 |
At a glance
- None 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