Likorall™ overhead lift 3122009Recalls & reported problems
Liko AB · Overhead track patient lifting/transfer system · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00887761979796), received between Mar 18, 2025 and Sep 26, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Fell” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Fell2
- Insufficient Device Problem Information2
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Erythema1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2025Insufficient Device Problem Information; Device Fell; Insufficient Device Problem Information; Device Fell
THE CUSTOMER REPORTED THAT "THE STRAP WAS DAMAGED AS A RESULT OF A FALL" THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23152966 ↗MalfunctionMar 18, 2025Device Fell; Device Fell
A CUSTOMER REPORTED THE LIKORALL 242 OVERHEAD LIFT MOTOR FELL ON THE FEMALE CAREGIVER CAUSING REDNESS TO HER RIGHT WRIST. TREATMENT WAS REPORTED AS APPLICATION OF HEMOCLAR CREAM. THERE WAS NO PATIENT IN THE LIFT AT THE TIME OF THE REPORTED EVENT.
Patient problems: Erythema
MAUDE report 21631417 ↗MalfunctionMar 18, 2025Detachment of Device or Device Component; Insufficient Device Problem Information; Detachment of Device or Device Component; Insufficient Device Problem Information
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 242 S, NATURAL, HAD AN ISSUE, CUSTOMER STATED THE SLING BAR IS DISENGAGED FROM THE STRAP. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21629785 ↗
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
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
- Uno™ mobile lift 2010004Liko AB · Lift, patient, non-ac-powered1 recall7 reports
- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
- Viking™ M mobile lift 2040045Liko AB · Lift, patient, non-ac-powered51 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.