Stryker Arise 1000EX mattress, Part Number 2236000000
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | October 31, 2025 |
| Reported | December 17, 2025 |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Country / region | United States MI |
Hazard
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
Affected products
- Stryker Arise 1000EX mattress, Part Number 2236000000
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