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Open, Classified

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

FDA Recall Z-1015-2026 · Posted 2026-01-16

Recalling FirmMedline Industries, LP
Recall StatusOpen, Classified
Product CodeLLI
Date Initiated2025-11-26
Product Quantity35694 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.

Firm 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 [email protected].

Root Cause

Device Design

Distribution Pattern

US, CA, PA, GUAM, VI

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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