Medline MDS88200DLBRecalls & reported problems
Medline Industries, Inc. · LIFT,PATIENT,HYDRAULIC, LOW BASE · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10888277362444), received between Jan 12, 2023 and Sep 30, 2026 — classified as 1 injury, 10 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (6 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Twisted/Bent6
- Fracture2
- Appropriate Device Problem Term/Code Not Available1
- Decrease in Pressure1
- Material Separation1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
- Fall1
- Laceration(s)1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Twisted/Bent
It was reported that "this lift, it completely bent while the patient was in it."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946043 ↗MalfunctionSep 29, 2026Material Twisted/Bent
It was reported that LIFT BASE IS BENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931814 ↗MalfunctionSep 18, 2026Decrease in Pressure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50822102 ↗MalfunctionSep 14, 2026Material Twisted/Bent
It was reported that "See photos attached of bent lift."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756164 ↗MalfunctionSep 10, 2026Material Twisted/Bent
Patient problems: Fall
MAUDE report 50724518 ↗MalfunctionSep 9, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50694366 ↗MalfunctionSep 9, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50692716 ↗MalfunctionSep 4, 2026Fracture; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50619739 ↗MalfunctionSep 1, 2026Material Twisted/Bent
It was reported that "Lift base is bent."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50548808 ↗MalfunctionAug 13, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50234262 ↗InjuryJan 12, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER "ONE OF THEIR STAFF WAS ASSEMBLING THE LIFT AND THEIR FINGER WAS PARTIALLY SEVERED OFF".
Patient problems: Laceration(s)
MAUDE report 16148215 ↗
Other Lift, patient, non-ac-powered devices
- MEDLINE MDS88200DMedline Industries, Inc. · Lift, patient, non-ac-powered108 reports
- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
- Uno™ mobile lift 2010004Liko AB · Lift, patient, non-ac-powered1 recall7 reports
- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
- Viking™ M mobile lift 2040045Liko AB · Lift, patient, non-ac-powered51 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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