Quick Facts at a Glance
- Recall Date
- October 31, 2025
- Hazard Level
- HIGH
- Brand
- Stryker Medical Division of Stryker
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Stryker Medical Division of Stryker
- Product type
- Hospital Mattress
- Model numbers
- GTIN 00857268006608, Serial Numbers: 1000502893, 1000281054, 1000281055, 1000281056, 1000213521, 1000213522, 1000213529 +12 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
October 31, 2025
Reported by FDA DEVICE
December 17, 2025
RecallRadar source check
December 24, 2025
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should stop using the affected mattresses immediately. This recall may create inconvenience but prioritizes patient safety.
Practical Guidance
How to identify if yours is affected
- Check the part number on the mattress, which should be 2236000000.
- Verify the serial number against the list provided in the recall notice.
- If in doubt, contact Stryker or your healthcare provider.
Where to find product info
The part number and serial numbers are typically found on the mattress tag or label.
What timeline to expect
Expect a refund processing timeline of 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document your attempts to contact Stryker.
- Follow up with a written letter or email if there is no response within a week.
How to prevent similar issues
- Always verify compatibility when purchasing medical devices and accessories.
- Check for recalls regularly on the manufacturer's website.
- Consult with healthcare professionals regarding equipment safety.
Documentation advice
Keep records of your purchase, correspondence with Stryker, and any photos of the mattress.
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Product Details
The recall includes Stryker Arise 1000EX mattresses with part number 2236000000. These mattresses were distributed in the United States and sold nationwide.
Key Facts
- Sold nationwide in the US
- High hazard level
- Class II recall
- Stop use immediately
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Safety Guide
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