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 10080196546992, 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 Low Basic Homecare Bed is designed for patient comfort and mobility in homecare settings. Consumers buy this product to provide a safe and adjustable sleeping environment for individuals with limited mobility.
Why This Is Dangerous
The hazard arises from the potential for the hand control pendant and wires to overheat, which can occur if the bed is misused or obstructed. This overheating can lead to serious fire risks, including sparking and burning.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the affected beds to prevent fire hazards. This may create inconvenience for users who rely on these beds for medical needs.
Practical Guidance
How to identify if yours is affected
- Verify if the model matches REF MDR107003ELO.
- Check for any signs of damage on the pendant or wires.
- Review any communication from Medline regarding the recall.
Where to find product info
The model number is typically found on the bed's frame or under the mattress.
What timeline to expect
Expect 4-6 weeks for refund processing after returning the bed.
If the manufacturer is unresponsive
- Follow up with Medline Industries via phone or email.
- File a complaint with the CPSC if necessary.
How to prevent similar issues
- Always check for recalls before purchase.
- Ensure proper use according to the manufacturer's guidelines.
- Inspect medical devices regularly for wear and tear.
Documentation advice
Keep records of your purchase, any communications with Medline, and photos of the product for your records.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
Product Details
The recalled product is the Full Electric Low Basic Homecare Bed, REF MDR107003ELO. A total of 22,565 units were distributed across the United States, Canada, Puerto Rico, Guam, and the Virgin Islands. These beds were sold through various healthcare providers.
Reported Incidents
Medline Industries received 58 complaints involving incidents of pendant sparking, burning, melting, or smoking. Fortunately, no injuries or deaths have been reported.
Key Facts
- Recall date: November 26, 2025
- Model: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
- Quantity recalled: 22,565 units
- Potential fire hazard from hand control pendant
- 58 complaints reported related to overheating
Browse More Recalls
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.