Medline MDSMR116Recalls & reported problems
Medline Industries, Inc. · SLING,MESH,FULL BODY,COMMODE,XL · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 10884389128770), received between Oct 1, 2020 and Sep 21, 2026 — classified as 3 injuries, 12 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (10 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
- Material Split, Cut or Torn10
- Material Integrity Problem3
- Material Separation2
- Adverse Event Without Identified Device or Use Problem1
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions10
- Fall3
- Insufficient Information1
- Laceration(s)1
- Limb Fracture1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50844191 ↗MalfunctionSep 10, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50722600 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50697390 ↗MalfunctionSep 8, 2026Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677882 ↗MalfunctionSep 7, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50656930 ↗MalfunctionSep 2, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50573886 ↗MalfunctionSep 1, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50543223 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50531761 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50531419 ↗MalfunctionJul 30, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50090177 ↗MalfunctionJun 3, 2026Material Separation; Material Integrity Problem
IT WAS REPORTED THAT, "THE PATIENT WAS BEING TRANSFERRED VIA HOYER WITH THE APPROPRIATE SLING FOR THE PATIENT'S WEIGHT FROM SHOWER CHAIR TO THE BED. THE SLING WAS WET FROM SHOWER" AND "THE SLING SNAPPED MID AIR".
Patient problems: Fall; Laceration(s)
MAUDE report 25375899 ↗MalfunctionMay 29, 2026Material Integrity Problem
IT WAS REPORTED THAT THE "SLINGS ARE SNAPPING".
Patient problems: Insufficient Information
MAUDE report 25337821 ↗InjuryMay 13, 2026Break; Material Integrity Problem
ACCORDING TO THE FACILITY, "WE HAD A RESIDENT BEING TRANSFERRED WITH A TOTAL LIFT SLING. THE RESIDENT WEIGHS 275# BOTH LOWER LEG LOOPS BROKE DURING TRANSFER DROPPING THE RESIDENT.
Patient problems: Fall
MAUDE report 25164257 ↗InjuryJan 6, 2026Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE CUSTOMER, THE SLING LOOP CAME UNHOOKED FROM THE LIFT, THE PATIENT FELL, WAS HOSPITALIZED, AND NEEDED STITCHES. ADDITIONALLY, IT WAS REPORTED WHILE USING A LIFT TO LIFT ANOTHER PATIENT, THE SLING LOOP CAME UNHOOKED FROM THE LIFT, THE PATIENT FELL, HIT THEIR HEAD, AND THE PATIENT DIED.
Patient problems: Fall
MAUDE report 23982043 ↗InjuryOct 1, 2020Material Split, Cut or Torn; Material Split, Cut or Torn
IT WAS REPORTED THAT THE SLING TORE AND THE RESIDENT FELL AND BROKE THEIR LEG.
Patient problems: Limb Fracture
MAUDE report 10614538 ↗
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
- 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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