Medline MDR107003LRecalls & reported problems
Medline Industries, Inc. · BED, 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.
Quick summary
This Medline MedLite electric hospital bed has 176 adverse event reports, with no deaths and 2 injuries. The reports mostly describe electrical faults, motors not raising one side or extending, noise, and mechanical jams. One recall is open, started in November 2025, over a potential hazard with the hand control and its wires in rare cases such as overloading the bed or a jammed motor. Reports rose to 174 in the latest 12 months from 2 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
- 198
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 198 adverse event reports that list this exact device (DI 40080196294344), received between Dec 4, 2024 and Sep 30, 2026 — classified as 2 injuries, 196 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (57 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-1015-2026 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem57
- Material Twisted/Bent27
- Mechanical Problem24
- Fracture23
- Noise, Audible12
- Mechanical Jam10
- Mechanics Altered9
- Break6
Patient problems
- No Clinical Signs, Symptoms or Conditions195
- Insufficient Information2
- Bone Fracture(s)1
Recent adverse event reports
The 25 most recent of 198 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952776 ↗MalfunctionSep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951817 ↗MalfunctionSep 30, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950571 ↗MalfunctionSep 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937388 ↗MalfunctionSep 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935183 ↗MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933746 ↗MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933685 ↗MalfunctionSep 28, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50924353 ↗MalfunctionSep 28, 2026Fracture
It was reported that "Here¿s the three beds the power cords are broken."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916715 ↗MalfunctionSep 28, 2026Fracture
It was reported that "Here¿s the three beds the power cords are broken.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916596 ↗MalfunctionSep 27, 2026Noise, Audible; Damaged Thread
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909449 ↗MalfunctionSep 26, 2026Fracture; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50906498 ↗MalfunctionSep 25, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903409 ↗MalfunctionSep 25, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903367 ↗MalfunctionSep 25, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903356 ↗MalfunctionSep 25, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903335 ↗MalfunctionSep 25, 2026Insufficient Device Problem Information
Customer stated "the headboard stopped raising".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50901305 ↗MalfunctionSep 24, 2026Electrical /Electronic Property Problem
It was reported that "I¿ve got a hospital bed with a broken foot motor. The electric motor portion runs, but the shaft will not extend or retract."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885047 ↗MalfunctionSep 24, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884588 ↗MalfunctionSep 24, 2026Fracture; Material Twisted/Bent
It was reported that "FLD18050039 has a cracked/bent frame on the Foot Spring Assembly near the area where it attaches to the Head Spring Assembly. FLD22030166 has a bent/twisted frame on the Foot Spring Assembly that does not allow left side to lie flat. FLD21020053 has a bent/twisted frame on the Foot Spring Assembly such that the end of the right side sits higher than the left and the left side does not lie flat."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50881928 ↗MalfunctionSep 23, 2026Damaged Thread
It was reported that "We have a hospital bed with a broken foot motor" and "Foot motor worm gear has broken, allowing the foot section to drop. Motor continues to run, but motor shaft does not move."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873009 ↗MalfunctionSep 23, 2026Damaged Thread
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872961 ↗MalfunctionSep 23, 2026Fracture
It was reported that "the right side of the foot section is not lifting up" and "the footboard has a broken pulley. When using the hi/lo function, one side of the footboard will raise and the other side does not."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870331 ↗MalfunctionSep 23, 2026Fracture
It was reported that "The main cord that plugs into the wall, the prongs broke off."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50868316 ↗MalfunctionSep 22, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50861036 ↗
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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