PlainRecalls
FDA Devices Critical Class I Ongoing

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

Reported: January 28, 2026 Initiated: November 26, 2025 #Z-1015-2026

Product Description

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

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.

Details

Recalling Firm
Medline Industries, LP
Units Affected
35694 units
Distribution
US, CA, PA, GUAM, VI
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L. Recalled by Medline Industries, LP. Units affected: 35694 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 28, 2026. Severity: Critical. Recall number: Z-1015-2026.