Medline MDSMSA2Recalls & reported problems
Medline Industries, Inc. · SLING,STAND ASSIST,DELUXE PADDED,MEDI · 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 10080196361199), received between Aug 31, 2026 and Sep 4, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50614231 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
It was reported that the slings are fraying and have loose threads.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50524448 ↗
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- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
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- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.