FDA Medical Device Recalls (openFDA)
Medline Industries, LP: MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
- Recall number
- Z-1012-2026
- Recalling firm
- Medline Industries, LP
- Product
- MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
- Status
- Open, Classified
- Initiated
- 2025-11-26
- Posted
- 2026-01-16
- Terminated
- not on file
- 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.com.
- Quantity
- 13245 units
- Distribution
- US, CA, PA, GUAM, VI
- Lot, serial or model codes
- UDI/DI 40080196294320, All lots
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LLI
- Firm FEI
- 1417592
- Firm city
- Northfield
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28