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Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Industries recalled 373,392 homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant can overheat, causing sparking or burning. The recall affects models MDR107002E and MDR107002E-4 sold in the U.S. and Canada.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) UDI/DI 40080196320999All lots2) UDI/DI 40080196320999

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
November 26, 2025
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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
Semi Electric Homecare Bed
Model numbers
1) UDI/DI 40080196320999, All lots, 2) UDI/DI 40080196320999, All Lots
Sold at
Multiple Retailers
Where affected
CA, PA, VI

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    November 26, 2025

  2. Reported by FDA DEVICE

    January 28, 2026

  3. RecallRadar source check

    February 4, 2026

  4. 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 Basic Homecare Bed is designed for patients who require assistance in adjusting their sleeping positions for comfort and medical needs. Consumers purchase these beds for home healthcare usage or for caregivers to provide better care.

Why This Is Dangerous

The hand control pendant can overheat under specific circumstances, such as exceeding the weight limit, which may lead to sparking or fire. Users should cease operation to prevent potential fire hazards.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using these beds immediately to avoid fire risks, which could lead to significant safety concerns and potential property damage.

Practical Guidance

How to identify if yours is affected

  1. Check the model number on the hand control pendant or bed frame.
  2. Look for the REF numbers: MDR107002E or MDR107002E-4.
  3. Confirm the purchase date to see if it falls within the recall timeframe.

Where to find product info

The model number and REF number can typically be found on a label attached to the hand control pendant or the bed frame itself.

What timeline to expect

Expect a response regarding refunds or replacements within 4-6 weeks after contacting Medline Industries.

If the manufacturer is unresponsive

  • Document all correspondence with Medline Industries.
  • Follow up via email or phone to escalate your request.
  • File a complaint with the CPSC if necessary.

How to prevent similar issues

  • Check for safety certifications like UL or CPSC compliance when purchasing medical devices.
  • Choose products with robust safety features and good consumer reviews.
  • Consider a manual option if concerned about electrical hazards.

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 products include the Semi Electric Basic Homecare Bed, REF MDR107002E, and the 4-pack version, REF MDR107002E-4. These beds were sold in the U.S., Canada, Puerto Rico, Guam, and the U.S. Virgin Islands.

Reported Incidents

Medline received 58 complaints regarding issues with the hand pendant, including sparking, burning, melting, and smoke. No injuries or deaths have been reported.

Key Facts

  • 58 reports of pendant issues
  • Risk of fire due to overheating
  • Stop using the product immediately
  • Contact Medline for recall instructions

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 Classification

Product Details

Model Numbers
1) UDI/DI 40080196320999
All lots
2) UDI/DI 40080196320999
All Lots
Affected States
CA, PA, VI
Report Date
January 28, 2026
Recall Status
ACTIVE

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