Medline MDSMR111Recalls & reported problems
Medline Industries, Inc. · SLING,MESH,FULL BODY,LARGE · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10884389128749), received between Jul 22, 2021 and Sep 30, 2026 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (4 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 Split, Cut or Torn4
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Hip Fracture1
- Limb Fracture1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950877 ↗MalfunctionSep 29, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934804 ↗MalfunctionSep 11, 2026Material Split, Cut or Torn
It was reported that one of the hooks for the sling is ripped.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50733212 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
It was reported that "Sling is tore on both sides."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50528738 ↗InjuryJul 22, 2021Break
IT WAS REPORTED; "THE STRAP ON THE SLING BROKE AND SHE FELL AND FRACTURE HER HIP."
Patient problems: Hip Fracture; Limb Fracture
MAUDE report 12211694 ↗
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- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
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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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