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.
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 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.
The hand control pendant and its associated wires can overheat under certain conditions, including exceeding the weight limit or encountering obstructions. In rare cases, this may result in sparking, burning, melting, smoking, or fire.
Medline Industries received 58 complaints involving incidents of pendant sparking, burning, melting, or smoking. Fortunately, no injuries or deaths have been reported.
Stop using the affected beds immediately. Contact Medline Industries for instructions regarding the recall and potential refund processes. Notifications have been sent to affected parties via letter.
For further information, call Medline Industries at [insert phone number] or visit their website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1014-2026.
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