WhichRecall
Class I — UrgentReported 2026-01-28

MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO

Recalled by Medline Industries, LP

Reason for Recall

Medline Industries has identified a potential hazard involving the hand control pendant and associated wires

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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.

Recall Number
Z-1016-2026
Classification
Class I
Status
Ongoing
Category
device
Initiated
2025-11-26
Reported
2026-01-28
Distribution
US, CA, PA, GUAM, VI
Code Info
UDI/DI 40080196325901, All lots
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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