Skip to content

Medline MDR107002ERecalls & reported problems

Medline Industries, Inc. · BED,BASIC, SEMI ELECTRIC · Class 2

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

Quick summary

This Medline semi-electric hospital bed has 322 reports, including 21 injuries and 1 death. Many describe electrical and power faults, and some mention the hand pendant not working, burns and electric shocks. It has 1 recall, still open since November 2025, over a possible hazard with the hand control pendant and its wires when the bed is overloaded, blocked or jammed. Reports rose to 286 in the last 12 months from 14 in the 12 months before.

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
374
Deaths reported
1
Injuries reported
21
Recalls naming it
1

Summary

The FDA's MAUDE database contains 374 adverse event reports that list this exact device (DI 40080196320999), received between Mar 6, 2019 and Sep 30, 2026 — classified as 1 death, 21 injuries, 351 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (114 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: 3 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 1 reportsMay 2024: 0 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 2 reportsOct 2024: 2 reportsNov 2024: 2 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 2 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 2 reportsJul 2025: 0 reportsAug 2025: 4 reportsSep 2025: 3 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 2 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 12 reportsMay 2026: 67 reportsJun 2026: 44 reportsJul 2026: 30 reportsAug 2026: 53 reportsSep 2026: 128 reportsOct 2026: 0 reports202420252026128
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-1011-2026 · Root cause: Device Design · FDA record ↗

Most reported problems

Device problems

  • Electrical /Electronic Property Problem114
  • Fracture32
  • Mechanical Problem24
  • No Apparent Adverse Event21
  • Material Twisted/Bent20
  • Material Frayed15
  • Power Problem14
  • Material Integrity Problem13

Patient problems

  • No Clinical Signs, Symptoms or Conditions342
  • Burn(s)5
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available4
  • Fall4
  • Electric Shock3
  • Insufficient Information3
  • Pain3
  • Abrasion2

Recent adverse event reports

The 25 most recent of 374 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Gas/Air Leak

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50953422 ↗
  • MalfunctionSep 30, 2026Material Integrity Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50952657 ↗
  • MalfunctionSep 30, 2026Break

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50951645 ↗
  • MalfunctionSep 30, 2026Material Twisted/Bent

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50949371 ↗
  • MalfunctionSep 30, 2026Fracture

    It was reported that the plastic shell of the motor is cracked and completely broken. It's not working at all.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50947078 ↗
  • MalfunctionSep 30, 2026Material Frayed

    It was reported that "WE SEE A LOOSE WIRE WITH THE REMOTE IT'S COVERED WITH BLACK MATERIAL, BUT WE CAN SEE THE WIRES NOW."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50946908 ↗
  • MalfunctionSep 30, 2026Material Twisted/Bent

    It was reported that "he is not able to raise or lower the bed using the crank" and "the customer inserted the crank and now it won't even come off anymore."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50945562 ↗
  • MalfunctionSep 30, 2026Material Twisted/Bent

    It was reported that "the bed is not working" and "they have to put pillows and boards to have the mattress on the bed even."

    Patient problems: Discomfort

    MAUDE report 50945519 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem; Material Frayed

    Bed remote is sparking fire.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50945223 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50938393 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50938390 ↗
  • MalfunctionSep 29, 2026Material Frayed

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50938014 ↗
  • MalfunctionSep 29, 2026Mechanical Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50937795 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50937790 ↗
  • MalfunctionSep 29, 2026Component Missing

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936683 ↗
  • MalfunctionSep 29, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934696 ↗
  • MalfunctionSep 29, 2026Material Frayed

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934197 ↗
  • MalfunctionSep 29, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50933743 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50933560 ↗
  • MalfunctionSep 29, 2026Material Twisted/Bent

    Patient problems: Cramp(s) /Muscle Spasm(s)

    MAUDE report 50933103 ↗
  • MalfunctionSep 29, 2026Fracture; Material Separation

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50933009 ↗
  • MalfunctionSep 29, 2026Fracture

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50932278 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    It was reported that the bed is no longer going up/down.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50932047 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    It was reported that the hand pendant stopped working. Replaced with a known good one and the bed works properly.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50927228 ↗
  • MalfunctionSep 28, 2026Unstable

    Patient problems: Abrasion

    MAUDE report 50925221 ↗

Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices

All BED, AC-POWERED ADJUSTABLE HOSPITAL devices →

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