Recall Z-0918-2026— Stryker Medical Division of Stryker Corporation
Class II · Ongoing
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2025-10-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Stryker MV3 bariatric bed, Part Number 5900000001. Reason: 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..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-10-31
- Firm location
- Portage, MI, United States
Product description
Stryker MV3 bariatric bed, Part Number 5900000001
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.