Stryker Medical Division of Stryker Corporation: Device Recall

Recall #Z-0918-2026 · 10/31/2025

Class II: Risk

Recall Details

Recall Number: Z-0918-2026
Classification: Class II
Product Type: Device
Recalling Firm: Stryker Medical Division of Stryker Corporation
Status: Ongoing
Date Initiated: 10/31/2025
Location: Portage, MI, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 294 units

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.

Product Description

Stryker MV3 bariatric bed, Part Number 5900000001

Distribution Pattern

US, nationwide

Other Recalls by Stryker Medical Division of Stryker Corporation

Class II: Risk 10/31/2025

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.

View all recalls by Stryker Medical Division of Stryker Corporation →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.