MEDLINE MDS88200DRecalls & reported problems
Medline Industries, Inc. · LIFT,PATIENT,HYDRAULIC,6 POINT CRADLE · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This is a Medline hydraulic patient lift with a six-point cradle, used to move people who cannot walk on their own. The 64 reports filed between May and August 2026 mostly describe metal parts breaking or bending, such as a cracked lifting shear and a hand pump that no longer works, plus mechanical sticking and electrical problems. There were 63 malfunctions, one injury and no deaths, and some reports mention falls. No recalls name this device.
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
- 108
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 108 adverse event reports that list this exact device (DI 40080196764250), received between May 18, 2026 and Sep 30, 2026 — classified as 1 injury, 106 malfunctions.
The most frequently reported specific device problem is “Fracture” (38 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
- Fracture38
- Material Twisted/Bent24
- Break9
- Loose or Intermittent Connection8
- Electrical /Electronic Property Problem7
- Mechanical Problem5
- Decrease in Pressure4
- Detachment of Device or Device Component4
Patient problems
- No Clinical Signs, Symptoms or Conditions98
- Fall8
- Back pain2
- Bruise/Contusion2
- Ambulation or Postural Difficulties1
- Balance Problems1
- Insufficient Information1
- Limb Pain1
Recent adverse event reports
The 25 most recent of 108 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952550 ↗MalfunctionSep 30, 2026Material Twisted/Bent
It was reported that ¿the lift valve is closed and its not pumping up.¿ It was also reported that ¿the replacement hydraulic cylinder received in not exactly the same,¿ ¿this one does not seem to pump up high enough,¿ and ¿With the lever released, it does not drop the boom arm.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50948768 ↗MalfunctionSep 30, 2026Loose or Intermittent Connection
It was reported that the wheel bearing broke off of of the lift.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947805 ↗MalfunctionSep 29, 2026Fracture; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932929 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916301 ↗MalfunctionSep 28, 2026Material Twisted/Bent; Mechanical Jam
It was reported that "one of the wheels is damaged. It looks like the wheel bearings got crimped at the manufacturer."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50913677 ↗MalfunctionSep 24, 2026Electrical /Electronic Property Problem
Patient problems: Ambulation or Postural Difficulties
MAUDE report 50891758 ↗MalfunctionSep 24, 2026Material Deformation
It was reported that "when someone is in the lift it is leaning on one side."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883919 ↗MalfunctionSep 23, 2026Material Twisted/Bent
It was reported that "caregiver trip over lift and noticed the lift base was bent."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872163 ↗MalfunctionSep 23, 2026Material Twisted/Bent
It was reported that "Bent base, picture attached."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870038 ↗MalfunctionSep 22, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50860916 ↗MalfunctionSep 22, 2026Fracture
It was reported that the lift fell apart and the metal part that holds the sling detached from the rest of the unit.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853970 ↗MalfunctionSep 21, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50847554 ↗MalfunctionSep 21, 2026Material Deformation
Patient problems: Back pain; Fall
MAUDE report 50846986 ↗MalfunctionSep 21, 2026Loose or Intermittent Connection
It was reported that "THE BREAKS STOPPED WORKING".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50844245 ↗MalfunctionSep 21, 2026Electrical /Electronic Property Problem
It was reported that the hydraulic pump on the lift does not work at all.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50843050 ↗MalfunctionSep 21, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50842646 ↗MalfunctionSep 21, 2026Fracture
It was reported that the bolt for the tie rod to the lift is sheared off.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50839752 ↗MalfunctionSep 21, 2026Fluid/Blood Leak; Fracture; Physical Resistance/Sticking
It was reported that "The retainer for the pump does not have a screw and the connect causing a failure in the lift."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50835143 ↗MalfunctionSep 18, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831106 ↗MalfunctionSep 18, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829308 ↗MalfunctionSep 18, 2026Material Twisted/Bent
It was reported that "their patient lift base has warped."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818018 ↗MalfunctionSep 17, 2026Loose or Intermittent Connection
Patient problems: Back pain; Bruise/Contusion; Fall
MAUDE report 50804625 ↗MalfunctionSep 16, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795184 ↗MalfunctionSep 16, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50788324 ↗
Other Lift, patient, non-ac-powered devices
- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- 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
- Likorall™ overhead lift 3122010Liko AB · Lift, patient, non-ac-powered1 recall13 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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