Medline MDSMR114Recalls & reported problems
Medline Industries, Inc. · SLING,FULL BODY MESH WITH COMMODE,MEDIU · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884389120637), received between Sep 7, 2026 and Sep 15, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (1 report).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Split, Cut or Torn1
- Sharp Edges1
Patient problems
- Localized Skin Lesion1
- No Clinical Signs, Symptoms or Conditions1
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Sharp Edges
It was reported that ¿by the seam around the opening has become very irritating to the skin as well as digs into the skin¿ and ¿The seams on the sling are hard sharp like coorse sand paper.¿
Patient problems: Localized Skin Lesion; Skin Inflammation/ Irritation
MAUDE report 50775280 ↗MalfunctionSep 7, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50657154 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.