MEDLINE beds labeled as: 1) Full 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) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pa…
- Recall number
- Z-1013-2026
- 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) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
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