Device recall
Z-2240-2011: Stryker, Impression, Non-Powered Mattress, Model 2980, Stryker Medical, Portage…
FDA device recall · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2240-2011 |
|---|---|
| Recall event | 58487 |
| Product | Stryker, Impression, Non-Powered Mattress, Model 2980, Stryker Medical, Portage, MI. The Impression non-powered mattress is recommended for use in the prevention of pressure ulcers. It is intended for use on Stryker frames and on other frames supporting a 84" x 35" x 6" mattress. |
| Product code | IKY |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2011 |
| 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