Stryker recalled 289 Arise 1000EX mattresses on October 31, 2025. The recall affects products sold nationwide due to potential incompatibility with MV3 beds. Users should stop using these mattresses immediately.
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.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Stryker Medical Division of Stryker Corporation or your healthcare provider for instructions. Notification method: Letter
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The Stryker Arise 1000EX mattress is designed for use in healthcare settings, particularly in hospitals for patient care. Consumers typically buy these mattresses for their durability and comfort in medical environments.
The recall arises from the potential incompatibility of the Arise 1000EX mattress with MV3 beds. The combination of these products has not been tested, which could pose safety risks to patients.
This recall is not part of a broader industry pattern.
Consumers should stop using the affected mattresses immediately. This recall may create inconvenience but prioritizes patient safety.
The part number and serial numbers are typically found on the mattress tag or label.
Expect a refund processing timeline of 4-6 weeks after returning the product.
Keep records of your purchase, correspondence with Stryker, and any photos of the mattress.
The recall includes Stryker Arise 1000EX mattresses with part number 2236000000. These mattresses were distributed in the United States and sold nationwide.
Not sure what to do next? Our guide walks you through the process step by step.
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