FDA Enforcement
Class I
Ongoing
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Recall: Z-1016-2026
·
Reported January 28, 2026
Enforcement
- Recall Number
- Z-1016-2026
- Event ID
- 98185
- Classification
- Class I
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Medline Industries, LP
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- January 28, 2026
- Initiation Date
- November 26, 2025
- Classification Date
- January 16, 2026
- Address
- 3 Lakes Dr, Northfield, IL, 60093-2753, United States
Description
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Reason
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.
Code Info
UDI/DI 40080196325901, All lots
Distribution
US, CA, PA, GUAM, VI
Quantity
15581 units