Likorall™ overhead lift 3122012Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00887761979468), received between Feb 1, 2022 and Jan 20, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Component Missing” (1 report).
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
- Component Missing1
- Device Fell1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 20, 2026Device Fell
ON 23-DEC-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 242 S R2R, WHITE (PRODUCT CODE 3122012, SERIAL NUMBER (B)(6)), LIFT WAS TRANSFERRING A PATIENT WHEN IT STOPPED WORKING AND LET GO OF THE PATIENT WHO WAS ABOVE THE WHEELCHAIR. 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 24120565 ↗MalfunctionJun 16, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
THE CUSTOMER REPORTED THAT A LIKORALL 242 LIFT WAS INVOLVED IN A PATIENT FALL. THE PICTURES PROVIDED BY THE CUSTOMER SHOWED THAT THE LIFT STRAP BROKE. DURING FOLLOW-UP THE CUSTOMER CONFIRMED THAT ¿THE PATIENT HAD SIMPLE BACK, SACRUM AND RIB PAIN, BUT AFTER X-RAY AND SCAN NOTHING ABNORMAL WAS FOUND¿.
Patient problems: Pain
MAUDE report 22211953 ↗MalfunctionFeb 1, 2022Component Missing; Component Missing
HILLROM RECEIVED A REPORT FROM THE ACCOUNT STATING THAT A PATIENT HAD FALLEN FROM THE LIFT. THE LIFT WAS LOCATED AT THE ACCOUNT AT THE TIME OF THE INCIDENT. THERE WAS NO PATIENT OR USER INJURY. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13415037 ↗
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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