Likorall overhead liftRecalls & reported problems across all models
Liko AB · 25 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one Likorall overhead lift model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 116
- Deaths reported
- 2
- Injuries reported
- 7
- Recalls
- 1
We found 25 models of Likorall overhead lift by Liko AB in the FDA's device registry (GUDID). Together they are named in 116 adverse event reports in the FDA's MAUDE database, received between Aug 15, 2021 and Sep 10, 2026 — classified as 2 deaths, 7 injuries, 107 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (52 reports).
1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Likorall overhead lift recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- 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 · names 25 of these models · Recall details · FDA record ↗
Most reported Likorall overhead lift problems
Device problems
- Mechanical Problem52
- Detachment of Device or Device Component16
- Device Fell13
- Insufficient Device Problem Information13
- Fracture8
- Break7
- Use of Device Problem4
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions94
- Fall10
- Hematoma6
- Head Injury5
- Pain4
- Insufficient Information3
- Laceration(s)2
- Nausea2
Likorall overhead lift models
25 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Likorall™ overhead lift 3123001Lift, patient, non-ac-powered1 recall1 death32 reports
- Likorall™ overhead lift 3121001Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Lift, patient, non-ac-powered1 recall18 reports
- Likorall™ overhead lift 3122010Lift, patient, non-ac-powered1 recall13 reports
- Likorall™ overhead lift 3122502Lift, patient, non-ac-powered1 recall5 reports
- Likorall™ overhead lift 3122011Lift, patient, non-ac-powered1 recall4 reports
- Likorall™ overhead lift 3123002Lift, patient, non-ac-powered1 recall4 reports
- Likorall™ overhead lift 3122012Lift, patient, non-ac-powered1 recall3 reports
- Likorall™ overhead lift 3122007Lift, patient, non-ac-powered1 recall3 reports
- Likorall™ overhead lift 3122009Lift, patient, non-ac-powered1 recall3 reports
- Likorall™ overhead lift 3122008Lift, patient, non-ac-powered1 recall2 reports
- Likorall™ overhead lift 3122011NALift, patient, non-ac-powered1 recall1 report
- Likorall™ overhead lift 3122501Lift, patient, non-ac-powered1 recall1 death1 report
- Likorall™ overhead lift 3122501NALift, patient, non-ac-powered1 recall1 report
- Likorall™ overhead lift 3123001NALift, patient, non-ac-powered1 recall1 report
- Likorall™ overhead lift 3122005Lift, patient, non-ac-powered1 recall1 report
- Likorall™ overhead lift 3122012NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122502NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3123002NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122005NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122006Lift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122006NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122007NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122008NALift, patient, non-ac-powered1 recall0 reports
- Likorall™ overhead lift 3122009NALift, patient, non-ac-powered1 recall0 reports
Recent Likorall overhead lift adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 10, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50722198 ↗MalfunctionSep 7, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50656934 ↗MalfunctionAug 6, 2026Device Fell
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50168542 ↗MalfunctionJul 13, 2026Break
Patient problems: Insufficient Information
MAUDE report 25807833 ↗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 ↗DeathJul 2, 2026Misconnection
IT WAS REPORTED THAT THE DURING PATIENT TRANSFER USING LIKORALL 243 LIFT, THE Q-LINK DISENGAGED FROM THE LIFT, RESULTING IN PATIENT FALLING AND STRIKING THEIR HEAD, AND SUBSEQUENTLY DIED. IT WAS REPORTED THAT THE PATIENT WAS INITIALLY TRANSFERRED FROM BED TO A TOILET SEAT USING THE LIFT. AFTER POSITIONING THE PATIENT ON THE TOILET SEAT, THE LIFT WAS LOWERED AND REMAINED IN THE LOWERED POSITION FOR A PERIOD OF TIME. WHEN STAFF RESUMED OPERATION AND ATTEMPTED TO LIFT THE PATIENT FROM THE TOILET SEAT, THE LIFT¿S SLING BAR BECAME DISENGAGED, RESULTING IN THE PATIENT FALLING. THE CUSTOMER STATED THE PATIENT HAD FALLEN AND SUSTAINED IMPACT TO THE ELBOW AND HEAD, RESULTING IN A CONTUSION, FOLLOWED BY DEATH. NO FURTHER INFORMATION REGARDING MEDICAL INTERVENTIONS REQUIRED AND PATIENT¿S ADMITTING DIAGNOSIS WAS PROVIDED. IT WAS NOT REPORTED IF AN AUTOPSY WAS PERFORMED. AN INSPECTION OF THE LIFT PERFORMED BY A BAXTER TECHNICIAN NOTED THAT THE LIFT¿S Q-LINK LATCH MECHANISM WAS FOUND TO BE IN GOOD CONDITION. NO VISIBLE DAMAGE OR DEFECT WAS OBSERVED AT THE TIME OF INSPECTION. THERE WAS NO DEVICE MALFUNCTION NOR PHYSICAL DAMAGE IDENTIFIED UPON INSPECTION, AND IT CANNOT BE EXCLUDED THAT THE EVENT W
Patient problems: Head Injury
MAUDE report 25700355 ↗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 ↗MalfunctionJun 16, 2026Fracture
BAXTER RECEIVED A REPORT THAT LIKORALL 242 S, WHITE HAD MOTOR HOOK BROKEN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25522550 ↗MalfunctionJun 10, 2026Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT LIKORALL 250 S, NATURAL, IRC HAD COMPOSITE HOOK BROKEN FROM SLING BAR. THIS OCCURRED DURING PATIENT USE. IT WAS REPORTED THAT THERE WAS NOT PATIENT/USER INJURY OR MEDICAL INTERVENTION WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25460591 ↗MalfunctionJun 1, 2026Fracture
BAXTER RECEIVED A REPORT THAT LIKORALL 250 S, NATURAL, IRC HAD BROKEN SLINGBAR HOOK. 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 25356222 ↗MalfunctionMay 7, 2026Fracture
BAXTER RECEIVED A REPORT THAT LIKORALL 250 ES, WHITE HAD SLING BAR HOOK BROKEN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25114207 ↗MalfunctionApr 7, 2026Detachment of Device or Device Component; Device Fell
BAXTER RECEIVED A REPORT THAT LIKORALL 200 HAD A CEILING STRAP DETACHMENT, IT SUDDENLY DROPPED. 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 24811018 ↗MalfunctionMar 30, 2026Detachment of Device or Device Component
BAXTER RECEIVED A REPORT THAT LIKORALL 250 S, NATURAL, IRC HAD A PLASTIC CLOSURE BECOME LOOSE WHILE LIFTING A PATIENT. THE PATIENT WAS TRANSFERRED TO THE BED SAFELY . 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 24720334 ↗MalfunctionMar 24, 2026Device Fell
ON 26-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 200 (PRODUCT CODE 3121001, SERIAL NUMBER (B)(6)), ONE HOOK ON THE SLINGBAR BREAKS. THE PATIENT FALLS DOWN ON THE BED. 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 24681057 ↗MalfunctionMar 9, 2026Device Fell
ON 12-FEB-2026, A DISTRIBUTOR CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 200 (PRODUCT CODE 3121001, SERIAL NUMBER (B)(6)), FALL OCCURRED DURING PATIENT TRANSFER. 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 24553502 ↗
Other Liko AB products
All Liko AB devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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