Likorall™ overhead lift 3122008Recalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887761979772), received between Jun 30, 2022 and Mar 3, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Use of Device Problem1
Patient problems
- Head Injury1
- Hematoma1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 3, 2025Break; Break
BAXTER RECEIVED A CUSTOMER COMPLAINT REPORTING THE LIKORALL 242 ES R2R, HAD A SHAFT BREAKAGE WHERE THE USER HAS FALLEN BACK DOWN INTO THEIR STANDING SUPPORT. 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 21503018 ↗InjuryJun 30, 2022Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT DURING USE OF A LIKORALL OVERHEAD LIFT WITH A LIKOSCALE, THE QUICK RELEASE HOOK OF THE SLING BAR LOOSENED AND THEN RELEASED, CAUSING A (B)(6) PATIENT TO FALL TO THE FLOOR SUSTAINING A LARGE HEMATOMA TO THE OUTSIDE OF THE SKULL. THE PATIENT WAS TAKEN TO THE HOSPITAL, X-RAYS WERE PERFORMED ON BOTH THE HEAD AND FEMUR WITH NO FRACTURES OR BLEEDING NOTED INTRACRANIALLY. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).
Patient problems: Head Injury; Hematoma
MAUDE report 14872113 ↗
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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