Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
FDA Recall Z-3228-2026 · Posted 2026-10-01
Recalling FirmMedline Industries, LP
Recall StatusOpen, Classified
Product CodeFNJ
Date Initiated2026-08-14
Product Quantity771,127 total
Reason for Recall
Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.
Firm Action
Firm initially notified customers November 26, 2025. On August 14, 2026, the firm sent a follow-up letter which provides additional product SKU - Item numbers for the electrical system safety risks and additional important information related to the previous notices.
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
Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.