FDA DevicesClass I
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Published: January 28, 2026Recall ID: Z-1015-2026Category: devicesCountry: US
Reason for Recall / Hazard
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 & Identification
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Additional Source Details
| Field | Value |
|---|---|
| City | Northfield |
| State | IL |
| Event id | 98185 |
| Address 1 | 3 Lakes Dr |
| Code info | UDI/DI 40080196294344, All lots |
| Postal code | 60093-2753 |
| Report date | 20260128 |
| Product type | Devices |
| Product quantity | 35694 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251126 |
| Initial firm notification | Letter |
| Center classification date | 20260116 |
Overview
- Recalling FirmMedline Industries, LP
- StatusOngoing
- Risk LevelClass I
- DistributionUS, CA, PA, GUAM, VI