MEDLINE beds labeled as: 1) Semi Electric Basic Homecare… recallZ-1011-2026 · Medline Industries, LP · initiated Nov 26, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Device Design
What the company is doing
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].
Recall details
- Recall number
- Z-1011-2026
- Status
- Open, Classified
- Initiated by the company
- Nov 26, 2025
- Posted by the FDA
- Jan 16, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 373392 units
- Product code
- LLI
- Distribution
- US, CA, PA, GUAM, VI
Product description
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
Code information (models, lots, serial numbers)
1) UDI/DI 40080196320999, All lots; 2) UDI/DI 40080196320999, All Lots
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Medline MDR107002EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death374 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98185).
- Z-1012-2026 · Open, ClassifiedMEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
- Z-1013-2026 · Open, ClassifiedMEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
- Z-1014-2026 · Open, ClassifiedMEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
- Z-1015-2026 · Open, ClassifiedMEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
- Z-1016-2026 · Open, ClassifiedMEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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