Medline Industries, LP: Device Recall
Recall #Z-1011-2026 · 11/26/2025
Class I: Dangerous
Recall Details
- Recall Number
- Z-1011-2026
- 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
- 373392 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: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
Distribution Pattern
US, CA, PA, GUAM, VI
Other Recalls by Medline Industries, LP
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
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.