Medline MDS600SABRecalls & reported problems
Medline Industries, Inc. · LIFT,PATIENT,STAND ASSIST,ELECTRC,600LB · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 10193489019278), received between Jul 29, 2026 and Sep 29, 2026 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (7 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem7
- Fracture2
- Battery Problem1
- Detachment of Device or Device Component1
- Failure to Charge1
- Failure to Power Up1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions13
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936751 ↗MalfunctionSep 17, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50804015 ↗MalfunctionSep 16, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794352 ↗MalfunctionSep 9, 2026Fracture; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701767 ↗MalfunctionAug 31, 2026Electrical /Electronic Property Problem
It was reported that "The lift is not raising to full height while staff is performing patient care. Example: - Resident on the lift -Lift begins to raise -Lift will not raise further and is not at full height -Staff attempt to lower and raise the lift -occasionally, after lowering and raising multiple times it will rise to full height -most times, the lift will not raise to full height".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50524437 ↗MalfunctionAug 14, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50253703 ↗MalfunctionAug 6, 2026Failure to Charge
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50165712 ↗MalfunctionAug 6, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50162579 ↗MalfunctionJul 31, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50104303 ↗MalfunctionJul 31, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50101824 ↗MalfunctionJul 30, 2026Battery Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50089838 ↗MalfunctionJul 30, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50084050 ↗MalfunctionJul 29, 2026Mechanical Jam
It was reported that the battery is holding a charge but the lift won't raise or lower and it's an issue with the hydraulics.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50069384 ↗
Other Lift, patient, non-ac-powered devices
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- Likorall™ overhead lift 3123001Liko AB · Lift, patient, non-ac-powered1 recall1 death32 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 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
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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