HIGH

Medline Recalls Homecare Beds Over Fire Hazard

Medline Industries recalled 22,565 Full Electric Low Basic Homecare Beds on November 26, 2025, due to a fire risk. The recall affects beds labeled with REF MDR107003ELO following 58 reports of overheating hand control pendants. Consumers should stop using the beds and follow recall instructions immediately.

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

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

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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

  1. Verify if the model matches REF MDR107003ELO.
  2. Check for any signs of damage on the pendant or wires.
  3. 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.

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

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
8/ 10
Affected Groups
GENERAL
Injury Types
BURN

Product Details

Model Numbers
UDI/DI 10080196546992
All lots
Affected States
CA, PA, VI
Report Date
January 28, 2026
Recall Status
ACTIVE

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