Medline Industries recalled 35,694 Full Electric Lightweight Homecare Beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat under certain conditions, leading to potential fire risks. The company received 58 complaints related to sparking and burning incidents.
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.
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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The Full Electric Lightweight Homecare Bed is designed to assist patients and healthcare providers in achieving comfort and mobility. These beds are commonly used in home healthcare settings to provide adjustable positioning for patients.
The hand control pendant can overheat in rare scenarios, particularly when the bed is overloaded or obstructed. This can lead to serious safety hazards, including the risk of fire.
This recall is not part of a broader industry pattern.
Consumers who own this bed must stop using it immediately, which could disrupt patient care. The potential fire risk necessitates urgent action.
The model number can usually be found on a label attached to the bed's frame or under the mattress support.
Expect refund processing to take around 4-6 weeks after contacting Medline.
Keep records of your purchase, including receipts and any correspondence with Medline regarding the recall.
The recalled product is the Full Electric Lightweight Homecare Bed, REF MDR107003L, with UDI/DI 40080196294344. Units were distributed in the US, Canada, Puerto Rico, Guam, and the Virgin Islands.
Medline Industries has received 58 complaints about the hand control pendant, including reports of sparking and burning. Fortunately, no injuries or fatalities have been reported.
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