FDA recall Z-1012-2026

Medline Industries, LP · Class I · device

Product

MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L

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.

Distribution

US, CA, PA, GUAM, VI

Key facts

Status
Ongoing
Initiation date
2025-11-26
Report date
2026-01-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1012-2026