Medline MDR107003ERecalls & reported problems
Medline Industries, Inc. · BED, BASIC, FULL 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 full electric hospital bed has 348 adverse event reports on file, including 3 deaths and 5 injuries. Many reports describe electrical and power problems and buttons that stop working. 1 open recall names this device: it began in November 2025 and concerns a possible hazard with the hand control and its wires in rare cases such as overloading the bed or a jammed motor. Reports in the last 12 months rose to 332 from 3 in the prior 12 months.
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
- 362
- Deaths reported
- 3
- Injuries reported
- 5
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 362 adverse event reports that list this exact device (DI 40080196321002), received between Nov 19, 2020 and Sep 30, 2026 — classified as 3 deaths, 5 injuries, 354 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (110 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
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-1013-2026 · Root cause: Device Design · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem110
- Mechanical Problem48
- Fracture28
- Noise, Audible24
- Power Problem18
- Mechanics Altered17
- Material Twisted/Bent14
- Key or Button Unresponsive/not Working13
Patient problems
- No Clinical Signs, Symptoms or Conditions334
- Insufficient Information14
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available5
- Abrasion2
- Electric Shock2
- Epistaxis1
- Erythema1
- Fall1
Recent adverse event reports
The 25 most recent of 362 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950972 ↗MalfunctionSep 30, 2026Material Frayed; Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949182 ↗MalfunctionSep 30, 2026Fracture; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50948911 ↗MalfunctionSep 30, 2026Fracture; Material Twisted/Bent
It was reported that "There are no functions of the bed that currently work." It was reported that "the cord is broken."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946524 ↗MalfunctionSep 30, 2026Failure to Align
It was reported that "The welding on beds makes it impossible for assembled bed to lay flat, the two pieces do not flush together. Resulting product is unusable because it sits at an angle."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946340 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938644 ↗MalfunctionSep 29, 2026Fracture; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935378 ↗MalfunctionSep 29, 2026Material Frayed
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934563 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934441 ↗MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934215 ↗MalfunctionSep 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934142 ↗MalfunctionSep 29, 2026Damaged Thread
It was reported that the head section will not raise and makes a grinding noise.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933909 ↗MalfunctionSep 29, 2026Failure to Align
It was reported that the head section will go up and down but the bed will not go back flat, has a raised lump in the middle. Also, stated that it appears that the footboard has dropped.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933824 ↗MalfunctionSep 29, 2026Deformation Due to Compressive Stress
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933659 ↗MalfunctionSep 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933138 ↗MalfunctionSep 29, 2026Fracture
It was reported that "The motor box broke and several pieces fell off and one side of the motor was hanging off the bed." It was also reported that "he heard a crack and the bed would not work by remote."
Patient problems: Paraplegia
MAUDE report 50932041 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
It was reported that "Bed will not go up and down."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931832 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem; Key or Button Unresponsive/not Working
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50930031 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem; Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50925129 ↗MalfunctionSep 28, 2026Accessory Incompatible
Patient problems: Abrasion; Epistaxis; Fall
MAUDE report 50922920 ↗MalfunctionSep 28, 2026Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917900 ↗MalfunctionSep 28, 2026Fracture; Material Twisted/Bent
It was reported that "The bar under the bed bent and broke the motor."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917645 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917001 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem; Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916663 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916050 ↗
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
- 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
- S3 3005Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall2 deaths242 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.