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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Home Healthcare

Medline Homecare Beds Recalled for Fire and Overheating Risk

Agency Publication Date: January 16, 2026
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Summary

Medline Industries is recalling 598,889 electric homecare beds due to a hazard where the hand control pendant and its wires can overheat. This overheating, which can occur if the bed is overloaded or the motor becomes jammed, poses a serious risk of fire. There have been 58 reports of the pendants sparking, melting, smoking, or catching fire. The recall affects several models of semi-electric and full-electric beds used in home settings.

Risk

The bed's hand control pendant and electrical cords can overheat and catch fire if the bed motor encounters an obstruction or is operated above its weight limit. Medline has received 58 complaints involving sparking, burning, and smoking pendants.

What You Should Do

  1. The recalled products include Medline Semi-Electric and Full-Electric Basic, Lightweight, and Low Homecare Beds. Identification labels on the bed frames contain the model (REF) and UDI/DI numbers.
  2. Check your bed's label for model numbers MDR107002E, MDR107002L, MDR107003E, MDR107003ELO, MDR107003L, or MDR107003LO. See the Affected Products section below for the full list of affected codes.
  3. Stop using the bed immediately if it is one of the affected models.
  4. Return the product to the place of purchase for a refund or replacement, throw it away, or contact Medline Industries for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional safety information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: Semi Electric Basic Homecare Bed
Variants: Standard, 4-pack
Model / REF:
MDR107002E
MDR107002E-4
Lot Numbers:
All lots
UDI:
40080196320999

Recall #: Z-1011-2026; Quantity: 373,392 units

Product: Semi Electric Lightweight Homecare Bed
Model / REF:
MDR107002L
Lot Numbers:
All lots
UDI:
40080196294320

Recall #: Z-1012-2026; Quantity: 13,245 units

Product: Full Electric Basic Homecare Bed
Variants: Standard, 4-pack
Model / REF:
MDR107003E
MDR107003E-4
Lot Numbers:
All lots
UDI:
40080196321002

Recall #: Z-1013-2026; Quantity: 138,412 units

Product: Full Electric Low Basic Homecare Bed
Model / REF:
MDR107003ELO
Lot Numbers:
All lots
UDI:
10080196546992

Recall #: Z-1014-2026; Quantity: 22,565 units

Product: Full Electric Lightweight Homecare Bed
Model / REF:
MDR107003L
Lot Numbers:
All lots
UDI:
40080196294344

Recall #: Z-1015-2026; Quantity: 35,694 units

Product: Full Electric Low Lightweight Homecare Bed
Model / REF:
MDR107003LO
Lot Numbers:
All lots
UDI:
40080196325901

Recall #: Z-1016-2026; Quantity: 15,581 units

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98185
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Medical equipment distributors; Homecare providers
Manufactured In: United States
Units Affected: 6 products (373392 units; 13245 units; 138412 units; 22565 units; 35694 units; 15581 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.