Device recall
Z-0942-2009: Stryker InTouch 1.0 Critical Care Bed (Model 2130) with the Integrated…
FDA device recall · Class II · Stryker Medical Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0942-2009 |
|---|---|
| Recall event | 49610 |
| Product | Stryker InTouch 1.0 Critical Care Bed (Model 2130) with the Integrated PositionPro mattress (Model 2920) option. The device is intended to be used as an Intensive Care Unit bed. |
| Product code | FNL |
| Recalling firm | Stryker Medical Div. of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 5, 2010 |
| 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