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
- ELDERLY
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 40080196294320, 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 Semi Electric Lightweight Homecare Bed is designed for patients who require assistance with mobility and positioning. It is commonly used in home care settings for elderly or disabled individuals.
Why This Is Dangerous
The hand control pendant may overheat in certain situations, leading to a fire risk if the bed is overloaded or obstructed. This overheating can cause the pendant and wiring to spark or melt.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the affected beds to prevent potential fire hazards, which can lead to serious injuries or property damage.
Practical Guidance
How to identify if yours is affected
- Check the model number on your bed to see if it matches REF MDR107002L.
- Look for the UDI/DI number 40080196294320 on the product label.
- Review any correspondence from Medline Industries regarding the recall.
Where to find product info
The model number and UDI/DI can usually be found on the bed's identification label, typically located on the frame or the control panel.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks once you have contacted Medline Industries.
If the manufacturer is unresponsive
- Document all communications with Medline Industries regarding the recall.
- Follow up with a phone call if you do not receive a timely response.
- Consider filing a complaint with regulatory agencies if no resolution is reached.
How to prevent similar issues
- Ensure any homecare bed purchased in the future complies with safety standards.
- Check for safety certifications from recognized authorities.
- Investigate product reviews and safety records before purchasing.
Documentation advice
Keep a record of your purchase receipt, any communications with Medline, and photos of the product for your records.
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Product Details
The recall involves Medline's Semi Electric Lightweight Homecare Bed, REF MDR107002L. It includes all lots under the model number UDI/DI 40080196294320. The beds were sold in the US, Canada, Puerto Rico, Guam, and the Virgin Islands.
Reported Incidents
Medline received 58 complaints related to the pendant overheating, resulting in sparking, burning, melting, or smoke. No injuries or deaths were reported.
Key Facts
- Quantity recalled: 13,245 units
- Hazard classification: Class I
- Risk of fire from hand control pendant
- Affected regions: US, CA, PA, GUAM, VI
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Safety Guide
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