Likorall™ overhead lift 3122501Recalls & 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
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761979482), received between Jul 3, 2026 and Jul 3, 2026 — classified as 1 death.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathJul 3, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE LIKORALL 250 ES LIFT (PRODUCT CODE 3122501, SERIAL NUMBER (B)(6) ALLEGEDLY MALFUNCTIONED DURING A PATIENT TRANSFER, RESULTING IN THE PATIENT FALLING ONTO THE BED. THE PATIENT REPORTEDLY SUSTAINED INJURIES AND SUBSEQUENTLY PASSED AWAY ON (B)(6) 2024. THE CAUSE OF DEATH WAS NOT REPORTED; NOR WAS IT CONFIRMED WHETHER THE FALL CONTRIBUTED TO THE PATIENT¿S DEATH. THE HOSPITAL¿S INTERNAL INVESTIGATION CONCLUDED THAT THE LIFT DID NOT CONTRIBUTE TO THE PATIENT¿S DEATH. A LATER INSPECTION IDENTIFIED A BROKEN MOTOR SPROCKET, WHICH WAS REPAIRED, AND THE DEVICE WAS FOUND TO BE FUNCTIONING AS DESIGNED. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Fall
MAUDE report 25706838 ↗
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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