Quick Facts at a Glance
- Recall Date
- November 26, 2025
- Hazard Level
- HIGH
- Brand
- Medline Industries, LP
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 3 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
- Medline Industries, LP
- Product type
- Homecare Bed
- Model numbers
- UDI/DI 40080196294344, All lots
- Sold at
- Multiple Retailers
- Where affected
- CA, PA, VI
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 26, 2025
Reported by FDA DEVICE
January 28, 2026
RecallRadar source check
February 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
About This Product
The Full Electric Lightweight Homecare Bed is designed to assist patients and healthcare providers in achieving comfort and mobility. These beds are commonly used in home healthcare settings to provide adjustable positioning for patients.
Why This Is Dangerous
The hand control pendant can overheat in rare scenarios, particularly when the bed is overloaded or obstructed. This can lead to serious safety hazards, including the risk of fire.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers who own this bed must stop using it immediately, which could disrupt patient care. The potential fire risk necessitates urgent action.
Practical Guidance
How to identify if yours is affected
- Locate the model number on the bed.
- Check if it matches REF MDR107003L or UDI/DI 40080196294344.
- Verify the recall status on the FDA website.
Where to find product info
The model number can usually be found on a label attached to the bed's frame or under the mattress support.
What timeline to expect
Expect refund processing to take around 4-6 weeks after contacting Medline.
If the manufacturer is unresponsive
- Document your communications with Medline.
- Follow up via phone or email to escalate the issue.
- Consider filing a complaint with the CPSC if unresponsive.
How to prevent similar issues
- Always check for recalls before purchasing a medical device.
- Ensure the weight limit is clearly marked and adhered to.
- Regularly inspect electrical components for signs of wear.
Documentation advice
Keep records of your purchase, including receipts and any correspondence with Medline regarding the recall.
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Product Details
The recalled product is the Full Electric Lightweight Homecare Bed, REF MDR107003L, with UDI/DI 40080196294344. Units were distributed in the US, Canada, Puerto Rico, Guam, and the Virgin Islands.
Reported Incidents
Medline Industries has received 58 complaints about the hand control pendant, including reports of sparking and burning. Fortunately, no injuries or fatalities have been reported.
Key Facts
- Recall date: November 26, 2025
- Quantity recalled: 35,694 units
- No reported injuries or deaths
- Affected in the US, Canada, Puerto Rico, Guam, VI
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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