Medline Industries, LP: Device Recall

Recall #Z-1016-2026 · 11/26/2025

Class I: Dangerous

Recall Details

Recall Number
Z-1016-2026
Classification
Class I
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
11/26/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15581 units

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.

Product Description

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

Distribution Pattern

US, CA, PA, GUAM, VI

Other Recalls by Medline Industries, LP

View all recalls by Medline Industries, LP →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.