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
- Bariatric Bed
- Model numbers
- GTIN 07613327419221. Serial Numbers: 2025013200138, 2025013200139, 2022013200001, 2022013200002, 2022013200003, 2021013200096, 2021013200098, 2021013200099 +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 MV3 bariatric bed is designed for patients who require a sturdy, adjustable bed for comfort and safety. Healthcare facilities commonly use these beds to support patients with specific medical needs.
Why This Is Dangerous
The recall was issued due to the sale of Stryker MV3 beds and Arise 1000EX mattresses in close proximity, which implies their intended use together. However, they have not been tested for compatibility, leading to potential safety hazards when used in conjunction.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the recalled beds immediately, which may result in inconvenience for healthcare providers and patients relying on these specific beds.
Practical Guidance
How to identify if yours is affected
- Locate the model number and serial number on your Stryker MV3 bed.
- Check the recall notice to see if your model is listed as affected.
- Contact Stryker Medical Division for clarification if needed.
Where to find product info
Model numbers and serial numbers can typically be found on the bed's frame or near the headboard area.
What timeline to expect
Expect a timeline of approximately 4-6 weeks for the processing of any refunds or replacements after following the recall instructions.
If the manufacturer is unresponsive
- Keep records of all communication with Stryker Medical.
- Contact the FDA if Stryker does not respond to your recall request.
How to prevent similar issues
- When purchasing medical devices, verify compatibility between products before use.
- Ensure that any combined products are from the same manufacturer or have been tested for compatibility.
Documentation advice
Keep a copy of the recall notice, receipts, and any correspondence with Stryker regarding the recall.
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Product Details
The recall affects Stryker MV3 bariatric beds, Part Number 5900000001. These beds were sold nationwide in the U.S. Specific model numbers include GTIN 07613327419221 and various serial numbers.
Key Facts
- Voluntary recall initiated on October 31, 2025
- Hazard classification: Class II
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Safety Guide
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