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Medline MDR107004Recalls & reported problems

Medline Industries, Inc. · BED,BARIATRIC,FULL ELECTRIC · Class 2

Quick summary

This Medline bariatric bed has 429 reports, including 12 injuries and no deaths. Most reports describe electrical and power faults, such as the bed not moving up or down, along with loud noise and worn parts. Reports rose sharply to 407 in the last year from 1 in the year before. No recalls name this device.

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
110
Deaths reported
0
Injuries reported
12
Recalls naming it
0

Summary

The FDA's MAUDE database contains 110 adverse event reports that list this exact device (DI 40080196321019), received between Nov 14, 2019 and Sep 30, 2026 — classified as 12 injuries, 98 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (31 reports).

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: 1 reportsApr 2024: 0 reportsMay 2024: 1 reportsJun 2024: 1 reportsJul 2024: 2 reportsAug 2024: 1 reportsSep 2024: 1 reportsOct 2024: 0 reportsNov 2024: 1 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: 1 reportsJan 2026: 3 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 3 reportsMay 2026: 14 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 7 reportsSep 2026: 60 reportsOct 2026: 0 reports20242025202660
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Electrical /Electronic Property Problem31
  • Fracture20
  • Material Twisted/Bent9
  • Appropriate Device Problem Term/Code Not Available8
  • Noise, Audible7
  • Fire5
  • Material Frayed5
  • No Apparent Adverse Event5

Patient problems

  • No Clinical Signs, Symptoms or Conditions91
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available4
  • Insufficient Information3
  • Bone Fracture(s)2
  • Fall2
  • Head Injury2
  • Limb Pain2
  • Ambulation or Postural Difficulties1

Recent adverse event reports

The 25 most recent of 110 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Mechanical Jam

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50952668 ↗
  • MalfunctionSep 30, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50952105 ↗
  • MalfunctionSep 30, 2026Moisture Damage

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50948334 ↗
  • MalfunctionSep 30, 2026Fracture

    It was reported that "HEAD FRAME BROKEN / BENT NOT WORKING."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50947014 ↗
  • MalfunctionSep 29, 2026Fracture

    It was reported that "Center shaft has fallen off and unable reinstall because of this broken part."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936945 ↗
  • MalfunctionSep 29, 2026Material Frayed

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936413 ↗
  • MalfunctionSep 29, 2026Damaged Thread

    It was reported that the head motor gears are stripped.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50935728 ↗
  • MalfunctionSep 29, 2026Material Twisted/Bent

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934038 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    It was reported that the bed/remote does not work. No power to the bed. They tried swapping out the cord with a different bed and also tried a different remote and nothing works.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934022 ↗
  • MalfunctionSep 28, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50924296 ↗
  • MalfunctionSep 28, 2026Detachment of Device or Device Component

    Patient problems: Fall

    MAUDE report 50922118 ↗
  • MalfunctionSep 28, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50917974 ↗
  • MalfunctionSep 28, 2026Electrical /Electronic Property Problem; Incomplete or Inadequate Connection

    Patient problems: Pain

    MAUDE report 50917925 ↗
  • MalfunctionSep 28, 2026Unstable; Detachment of Device or Device Component

    Patient problems: Fall; Head Injury; Limb Pain

    MAUDE report 50917559 ↗
  • MalfunctionSep 28, 2026Electrical /Electronic Property Problem

    This summary report covers malfunction events that occurred between July 1 and September 30, 2023. This VMSR summarizes one malfunction event involving two Medline full-electric bariatric beds (catalog/model number MDR107004). The account reported that the hand pendants on both beds were not working and that the button to lower either bed did not function. No devices or photos were returned or provided; therefore, the reported malfunction could not be confirmed. No patient information was available. No patient or user injuries were reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50914974 ↗
  • MalfunctionSep 25, 2026Electrical /Electronic Property Problem

    It was reported that the bed is not going up and down. When attempting to lower the bed there was a noise and then it stopped working.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50897397 ↗
  • MalfunctionSep 24, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50890369 ↗
  • MalfunctionSep 24, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50889786 ↗
  • MalfunctionSep 24, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50889210 ↗
  • MalfunctionSep 24, 2026Electrical /Electronic Property Problem; Loose or Intermittent Connection

    Patient problems: Diaphoresis

    MAUDE report 50889139 ↗
  • MalfunctionSep 24, 2026Fracture

    It was reported that "the motor towards the head section of the bed has come unattached." "Stated that recently when raising or lowering the head section of the bed he could feel a little bump" and "when he looked he saw the motor was no longer on the bed and a screw and spring were also on the ground."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50885522 ↗
  • MalfunctionSep 24, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50885014 ↗
  • MalfunctionSep 23, 2026Fracture

    It was reported that "The cable in the footboard is broken on the end user bed" and "the left side of the footboard is stuck all the way down and would not move."

    Patient problems: Ambulation or Postural Difficulties

    MAUDE report 50867750 ↗
  • MalfunctionSep 22, 2026Electrical /Electronic Property Problem; Noise, Audible

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50860341 ↗
  • MalfunctionSep 22, 2026Electrical /Electronic Property Problem

    It was reported that "Headboard fail. One side of the headboard will no longer raise or lower."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50855792 ↗

Other Bariatric bed devices

All Bariatric bed devices →

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