Stryker has issued a voluntary recall for 591 units of its MV3 bariatric beds and Arise 1000EX mattresses because these products have been sold in close proximity, suggesting they might be used together. However, these two products have not been tested for compatibility and are not designed to be used as a set. Stryker does not recommend using this specific bed and mattress combination because their performance together is unverified.
Using these products together could potentially lead to safety risks because the mattress and bed frame were not designed to work as a unified system. While no specific injuries have been reported, the lack of compatibility testing means patient stability or device function could be compromised.
Recall #: Z-0918-2026. Quantity: 294 units.
Recall #: Z-0919-2026. Quantity: 297 units.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.