Medical device recalls High risk

MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed recalled over fire hazard

Recall date
November 26, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Medline Industries, LP recalls MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pa…
Recall number
Z-1011-2026
FDA classification
Class I
Brand / firm
Medline Industries, LP
Sold / distributed
US, CA, PA, GUAM, VI

Why it was recalled

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.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4

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