Home/Recalls/FDA-Z-1012-2026
FDA DevicesClass I

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

Published: January 28, 2026Recall ID: Z-1012-2026Category: devicesCountry: US

Reason for Recall / Hazard

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.

Product Description & Identification

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

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98185
Address 13 Lakes Dr
Code infoUDI/DI 40080196294320, All lots
Postal code60093-2753
Report date20260128
Product typeDevices
Product quantity13245 units
Reason for recallMedline 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251126
Initial firm notificationLetter
Center classification date20260116

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS, CA, PA, GUAM, VI
Official Agency Alert