Liko LiftPants™, Mod. 92 3592327Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887761984028), received between Jan 14, 2025 and Jan 16, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (2 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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 16, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIFTPANTS 92 PES MESH XL HAD AN ISSUE, THE LIFT PANTS HAVE BEEN INSPECTED DURING AND HAVE FAILED. THE INSPECTOR STATED THE STRAP WAS TESTEDAT APPROX. 100KG, AND THE STRAP CAME APART THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21166908 ↗
• MalfunctionJan 14, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIFTPANTS 92 PES MESH XL, HAD AN ISSUE, DURING USE WITH A PATIENT THE STITCHING BECAME UNDONE AND CAUSED THE PATIENT TO DROP ABOUT 6 INCHES BACK ONTO THE CHAIR THEY WERE LIFTED FROM. NO INJURY WAS REPORTED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21151908 ↗