Stryker Medical Division of Stryker Corporation recalls Stryker Arise 1000EX mattress, Part Number 2236000000

Recall date

October 31, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0919-2026

FDA classification

Class II

Brand / firm

Stryker Medical Division of Stryker Corporation

Sold / distributed

US, nationwide

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Stryker Arise 1000EX mattress, Part Number 2236000000