Medical Device Recall: Stryker Arise 1000EX mattress, Part Number 2236000000
Stryker Medical Division of Stryker Corporation · October 31, 2025
Reason for Recall
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.
Distribution
US, nationwide
States Affected
NATIONWIDE
Quantity Affected
297 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0919-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.