HIGH

Stryker MV3 Bariatric Bed Recalled Over Compatibility Issues

Stryker Medical recalled 286 MV3 bariatric beds on October 31, 2025. The beds may not be compatible with Arise 1000EX mattresses, posing risks to patients. Healthcare providers and patients must stop using the beds immediately.

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

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

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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

  1. Locate the model number and serial number on your Stryker MV3 bed.
  2. Check the recall notice to see if your model is listed as affected.
  3. 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.

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

  • 286 units recalled
  • Voluntary recall initiated on October 31, 2025
  • Reported incidents: 0
  • Hazard classification: Class II

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
GTIN 07613327419221. Serial Numbers: 2025013200138
2025013200139
2022013200001
2022013200002
2022013200003
+15 more
Affected States
ALL
Report Date
December 17, 2025
Recall Status
ACTIVE

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