MEDLINE MDSMR113Recalls & reported problems
Medline Industries, Inc. · SLING,SOLID,FULL BODY,LARGE · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10884389128756), received between Aug 31, 2026 and Sep 29, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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
- Material Split, Cut or Torn7
- Material Discolored1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Fall2
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Material Split, Cut or Torn
It was reported that "The concern is the tags are completely coming off."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50927906 ↗MalfunctionSep 17, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810239 ↗MalfunctionSep 16, 2026Material Split, Cut or Torn
It was reported that "The concern is the tags are completely coming off."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793646 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50699191 ↗MalfunctionSep 4, 2026Material Discolored; Material Split, Cut or Torn
Patient problems: Fall
MAUDE report 50615191 ↗MalfunctionSep 2, 2026Material Separation; Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50569100 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
Patient problems: Fall
MAUDE report 50532402 ↗
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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