Medline Industries, LP recalls MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed
- Recalling company
- Medline Industries, LP
- Product
- MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
- 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.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Nov 26, 2025
- Reported
- Jan 28, 2026
- Distribution
- US, CA, PA, GUAM, VI
- Status
- Ongoing
- Quantity
- 35694 units
- Lot / codes
- UDI/DI 40080196294344, All lots
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1015-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1015-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.