Medline MDR107003LORecalls & reported problems
Medline Industries, Inc. · 2 PCS BED, LOW FULL ELECTRIC, MEDLITE · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 27
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 27 adverse event reports that list this exact device (DI 40080196325901), received between Mar 21, 2023 and Sep 30, 2026 — classified as 3 injuries, 24 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (13 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Recalls naming this device
- 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-1016-2026 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem13
- Material Twisted/Bent5
- Fracture4
- Appropriate Device Problem Term/Code Not Available2
- Noise, Audible2
- Failure to Align1
- Failure to Power Up1
- Material Frayed1
Patient problems
- No Clinical Signs, Symptoms or Conditions26
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 25 most recent of 27 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Electrical /Electronic Property Problem; Material Twisted/Bent
It was reported that "on the right side of the footboard, the leg will not lift up. Everything else is raising fine except for this corner."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50948128 ↗MalfunctionSep 30, 2026Mechanical Problem; Failure to Align; Noise, Audible
It was reported that "WHEN THE BED GOES UP AND DOWN THE HEADBOARD IS MAKING NOISE AND WHEN THE BOARD IS GOING UP AND DOWN THE BED BECOME UNLEVELED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947013 ↗MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937329 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
It was reported that "they are having issues with the bed not going down properly and stopping halfway down."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931533 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918779 ↗MalfunctionSep 28, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917180 ↗MalfunctionSep 25, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50904275 ↗MalfunctionSep 24, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50888987 ↗MalfunctionSep 23, 2026Fracture; Material Frayed
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872909 ↗MalfunctionSep 22, 2026Fracture; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856149 ↗MalfunctionSep 18, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829225 ↗MalfunctionSep 18, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829219 ↗MalfunctionSep 18, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829206 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809782 ↗MalfunctionAug 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50504693 ↗MalfunctionAug 27, 2026Noise, Audible
It was reported that the hi/lo motor is grinding and making a clicking noise. Customer removed the shaft to see if it was the shaft making the noise but it's the actual motor making the noise.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50475451 ↗MalfunctionAug 24, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50418254 ↗MalfunctionAug 12, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50229457 ↗MalfunctionAug 10, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50193536 ↗MalfunctionAug 7, 2026Electrical /Electronic Property Problem
It was reported that the bed 'will not stay in the position they want it in.' When it is raised, for example, it will not stay raised and will lower on its own.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50181387 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
It was reported that the foot motor on a MDR107003LO Low bed made a 'pop' noise and the foot section will not rise. Verified that the shaft does not appear to be connected to the motor internally.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50025668 ↗MalfunctionJun 19, 2026Electrical /Electronic Property Problem
IT WAS REPORTED THAT "HAND PENDANT NEEDS TO BE REPLACED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25568202 ↗MalfunctionMay 14, 2026No Apparent Adverse Event
CUSTOMER STATED "THE HEAD SECTION DOES NOT RAISE UP OR ELEVATE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25168023 ↗MalfunctionApr 15, 2026Mechanics Altered
IT WAS REPORTED THAT THE FOOTBOARD IS DEFECTIVE BED WILL NOT GO BACK UP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24891952 ↗InjuryMar 27, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER ON (B)(6), "A BOLT CAME OUT OF THE HEAD SECTION GATCH CAUSING THE HEAD TO COLLAPSE ON ONE SIDE AND THAT THE PATIENT WAS IN THE BED WITH THE HEAD RAISED WHEN THE INCIDENT OCCURRED".
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 18987218 ↗
Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices
- Centrella™ Bed P7900BHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL2 recalls5 deaths1,937 reports
- Progressa® Bed System P7500AHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death1,377 reports
- VersaCare® Med Surg Bed P3200KHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL3 deaths1,193 reports
- Medline MDR107002EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death374 reports
- Medline MDR107003EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall3 deaths362 reports
- InTouch 2141Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths361 reports
- Citadel Plus FX811B3B4AMABBArjohuntleigh AB · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths358 reports
- TotalCare® Bed P1900QHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL317 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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