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
- Electric Homecare Bed
- Model numbers
- UDI/DI 40080196325901, 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 Medline Full Electric Low Lightweight Homecare Bed is designed for patients requiring in-home care. Its electric operation allows for easy adjustments to accommodate patient needs.
Why This Is Dangerous
The hand control pendant and associated wires may overheat under specific conditions, which can lead to fire hazards. This issue arises when the bed is used improperly or encounters obstructions.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall necessitates immediate cessation of use and poses safety risks for patients and caregivers, leading to potential disruptions in care.
Practical Guidance
How to identify if yours is affected
- Check the model number on the bed for REF MDR107003LO.
- Verify if your bed is included in the recall by visiting the Medline website or contacting them.
- Look for any signs of damage or overheating in the hand control pendant.
Where to find product info
The model number can typically be found on a label on the base of the bed or near the hand control pendant.
What timeline to expect
Expect a refund or replacement to be processed within 4-6 weeks.
If the manufacturer is unresponsive
- Document your communication attempts with Medline.
- Contact your healthcare provider for assistance if Medline does not respond.
How to prevent similar issues
- Ensure proper usage of the bed according to manufacturer's specifications.
- Regularly inspect the hand control and cables for wear or damage before use.
Documentation advice
Keep all correspondence regarding the recall, including letters, receipts, and any communication with Medline.
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Product Details
The recalled product is the Full Electric Low Lightweight Homecare Bed, REF MDR107003LO. It was sold in the U.S., Canada, Puerto Rico, Guam, and the Virgin Islands.
Reported Incidents
Medline Industries received 58 reports of incidents involving the hand pendant, including sparking, burning, melting, and smoking.
Key Facts
- Recalled model: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
- Reported incidents: 58 complaints
- Recall date: November 26, 2025
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Safety Guide
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