Likorall™ overhead lift 3123002Recalls & reported problems
Liko AB · Overhead track patient lifting/transfer system · Class 1
All models of Likorall overhead lift (25)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761979543), received between Aug 26, 2024 and Sep 7, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Defective Component” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Sep 14, 2026Open, Classified
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.
Z-0151-2027 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Defective Component2
- Detachment of Device or Device Component1
- Device Fell1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 7, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50656934 ↗MalfunctionJul 1, 2026Device Fell
BAXTER RECEIVED A REPORT THAT LIKORALL 243 ES, WHITE HAD LIFT STRAP DROPPED DOWN WHEN WEIGHT IS APPLIED TO IT. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25686041 ↗MalfunctionSep 10, 2024Defective Component; Defective Component
THE SERVICE TECHNICIAN FOUND THAT WHILE PERFORMING ANNUAL PM TECHNICIAN FUNCTIONALLY INSPECTED THAT CPR FEATURE WOULD NOT ENGAGE. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF (B)(4)
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20182293 ↗MalfunctionAug 26, 2024Defective Component; Defective Component
THE SERVICE TECHNICIAN FOUND THAT WHILE PERFORMING ANNUAL PM TECHNICIAN FUNCTIONALLY INSPECTED THAT CPR FEATURE WOULD NOT ENGAGE. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20062757 ↗
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
- Likorall™ overhead lift 3123001Liko AB · Lift, patient, non-ac-powered1 recall1 death32 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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