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Medline MDR107003ELORecalls & reported problems

Medline Industries, Inc. · BED, LOW FULL ELECTRIC, BASIC · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Quick summary

This Medline basic low electric hospital bed has 66 reports, all describing malfunctions, with no deaths and no injuries. Most concern the hand control pendant and its wiring: buttons and controls that no longer respond, so the bed cannot be moved, plus electrical faults and mechanical jamming. One open recall, started in November 2025, cites a design hazard with the hand pendant and wires, which can fail in rare situations such as exceeding the bed's weight limit, an obstruction blocking bed movement, or a jammed motor.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
63
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 63 adverse event reports that list this exact device (DI 10080196546992), received between Aug 12, 2024 and Sep 30, 2026 — classified as 63 malfunctions.

The most frequently reported specific device problem is “Failure to Read Input Signal” (7 reports).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 2 reportsMay 2026: 6 reportsJun 2026: 28 reportsJul 2026: 3 reportsAug 2026: 10 reportsSep 2026: 13 reportsOct 2026: 0 reports20242025202628
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Nov 26, 2025Open, Classified

    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.

    Z-1014-2026 · Root cause: Device Design · FDA record ↗

Most reported problems

Device problems

  • Failure to Read Input Signal7
  • Electrical /Electronic Property Problem6
  • Mechanical Jam5
  • Noise, Audible5
  • Fracture4
  • Key or Button Unresponsive/not Working4
  • Mechanical Problem4
  • Insufficient Device Problem Information3

Patient problems

  • No Clinical Signs, Symptoms or Conditions62
  • Fall1

Recent adverse event reports

The 25 most recent of 63 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Material Frayed

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50952807 ↗
  • MalfunctionSep 30, 2026Key or Button Unresponsive/not Working

    It was reported that ¿the customer was calling due to receiving the recall notice. The pendant buttons do not work¿.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50946868 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem; Damaged Thread

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934385 ↗
  • MalfunctionSep 28, 2026Material Twisted/Bent

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50924066 ↗
  • MalfunctionSep 28, 2026Fracture

    It was reported that while moving the bed the prongs on the power cord broke off.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50915191 ↗
  • MalfunctionSep 28, 2026Detachment of Device or Device Component

    It was reported that the head portion of the bed wasn't working, the motor fell off from where it was mounted on the bed.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50913216 ↗
  • MalfunctionSep 25, 2026Activation Failure

    It was reported that the foot section of the patient's bed wasn't working.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50896112 ↗
  • MalfunctionSep 24, 2026Fracture

    It was reported that "Foot spring motor for hi-lo bed. When bed is raising the foot board is kicking out."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50888659 ↗
  • MalfunctionSep 24, 2026Fracture

    It was reported that "the bar snapped that caused the head section not to go up."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50883143 ↗
  • MalfunctionSep 23, 2026Overheating of Device

    It was reported that ¿intermittently has to push some more than once and the pendant becomes warm or hot to touch¿.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50870323 ↗
  • MalfunctionSep 23, 2026Fracture; Material Twisted/Bent

    It was reported that the bed frame was bent and the head motor required replacement. Review of photos showed a bent spring assembly arm and fractured paint at the weld. No injury was reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50868199 ↗
  • MalfunctionSep 17, 2026Mechanical Problem

    It was reported that "broken pully system."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50801090 ↗
  • MalfunctionSep 2, 2026Noise, Audible

    Customer stated "the motor makes an unusual noise when raising and lowering the unit on both sections (head and foot) of the bed."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50570038 ↗
  • MalfunctionAug 28, 2026Noise, Audible; Damaged Thread

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50501307 ↗
  • MalfunctionAug 27, 2026Loose or Intermittent Connection; Detachment of Device or Device Component

    It was reported that "MEMBERS HOSIPTAL BED REMOTE IS NO LONGER WORKING-THE ATTACHMENT IS NO LONGER ATTACHED TO THE REMOTE SO ALL MOVEMENT OF THE BED IS NOT ABLE TO WORK."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50480673 ↗
  • MalfunctionAug 27, 2026Electrical /Electronic Property Problem

    It was reported that "arrived with a broken motor and pendant."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50480574 ↗
  • MalfunctionAug 26, 2026Insufficient Device Problem Information

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50461887 ↗
  • MalfunctionAug 25, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50431065 ↗
  • MalfunctionAug 24, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50419525 ↗
  • MalfunctionAug 24, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50411769 ↗
  • MalfunctionAug 17, 2026Noise, Audible

    It was reported that the high low bar doesn t work and was making a squeaking sound.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50275256 ↗
  • MalfunctionAug 11, 2026Material Frayed; Overheating of Device; Material Integrity Problem

    It was reported that the pendant wiring is either damaged, fraying, or internal wires are exposed. Additionally, the customer contact reported that the pendant buttons do not work or are stuck, and the pendant becomes warm or hot to touch. The customer reported that they "received recall letter" and "there is a bolt on the foot part of the frame that is broken."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50213291 ↗
  • MalfunctionAug 11, 2026Material Integrity Problem

    It was reported that the prong of the cable for the bed coming out of the motor broke off, it was pulled out hard out of the outlet.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50212365 ↗
  • MalfunctionJul 27, 2026Positioning Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50001004 ↗
  • MalfunctionJul 27, 2026Activation Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50000828 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.