Recall Z-1016-2026 ยท LLI Bed, Therapeutic, Ac-Powered, Adjustable Home-Use
Medline Industries, LP
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
| Date | Jan 16, 2026 (initiated Nov 26, 2025) |
| Status | Open, Classified |
| 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. |
| Root cause | Device Design |
| Action | Medline issued an URGENT MEDICAL DEVICE RECALL notice with an enclosed URGENT MEDICAL DEVICE FIELD CORRECTION NOTICE to its consignees on 11/26/2025 via email and USPS first class mail. The notice explained the issue, potential risks, and requested the user ONLY USE MEDLINE SIDE RAILS and MEDLINE ACCESSORIES that are intended for use with Medline Homecare Beds. When using Medline Side Rails and Medline Accessories, follow all applicable instructions for use. Distributors were directed to notify their customers. For questions, contact the Recall Department at 866-359-1704 orrecalls@medline.co |
| Quantity | 15581 units |
| Distribution | US, CA, PA, GUAM, VI |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.