Medical Device Recall: MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Medline Industries, LP · November 26, 2025
Reason for Recall
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.
Distribution
US, CA, PA, GUAM, VI
States Affected
CA, PA
Quantity Affected
13245 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1012-2026
Status: ongoing
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