Likorall™ overhead lift 3122010Recalls & reported problems

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00887761979819), received between Feb 7, 2023 and Jun 16, 2026 — classified as 1 injury, 12 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• MalfunctionDec 18, 2025Insufficient Device Problem Information; Device Fell; Insufficient Device Problem Information; Device Fell

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 242 S, WHITE HAD AN ISSUE, AN ACCIDENT OCCURRED DUE TO ENGINE FAILURE. THE PERSON HAD A FALL. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23839561 ↗
• MalfunctionOct 6, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 242 S, WHITE HAD AN ISSUE, IT WAS REPORTED THE SLING BAR HOOK DETACHED FROM THE ADAPTER 22 DURING A TRANSFER LEADING TO A PATIENT FALL. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23227147 ↗
• MalfunctionSep 29, 2025Break; Insufficient Device Problem Information; Break; Insufficient Device Problem Information

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT DURING THE TRANSFER OF A RESIDENT, THE LOAD-BEARING STRAP FAILED. LUCKILY, THEY WERE ABOVE THE BED AT THE TIME OF THE INCIDENT, WHICH PREVENTED ANY INJURIES. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23165962 ↗
• MalfunctionSep 15, 2025Mechanical Problem; Insufficient Device Problem Information; Mechanical Problem; Insufficient Device Problem Information

  THE CUSTOMER REPORTED THAT A LIKORALL 242 LIFT WAS INVOLVED IN A PATIENT FALL. THE SEQUENCE OF EVENTS SURROUNDING THE FALL WAS NOT PROVIDED. HOWEVER, THE CUSTOMER REPORTED THAT THE PATIENT SUSTAINED A ¿BUMP ON THE HEAD¿ AND ¿FELL ON HIS BUTTOCKS.¿ MEDICAL INTERVENTION WAS NOT REPORTED.

  Patient problems: Fall; Hematoma

  MAUDE report 23051156 ↗
• MalfunctionSep 11, 2025Material Split, Cut or Torn; Material Split, Cut or Torn

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT THE LIKORALL 242 S, CHARGER WAS DAMAGED WITH EXPOSED COPPER.THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23027647 ↗
• MalfunctionAug 12, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 242 S, WHITE, HAD AN ISSUE, SUSPICION OF THE SLINGBAR HARNESS COMING OUT OF THIS LIKORALL 242S ENGINE. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22786994 ↗
• MalfunctionMay 14, 2025Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 242 S, WHITE HAD AN ISSUE, WHEN INSPECTING A LIKORAL 242'S LIFT, THE LIFTSTRAP WAS CHANGED AND WHEN TESTING THE MANUAL EMERGENCY LOWERING, THE LIFT STRAP SLID UNCONTROLLABLY STRAIGHT THROUGH AT FIRST ¿HAND PUMPING¿. USUALLY YOU GET TO ¿PUMP¿ DOWN TYPE 6-7 CM AT A TIME AT 60 KG SAMPLE WEIGHT. THIS OCCURRED DURING BIOMED TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22016856 ↗
• InjuryMar 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED A PATIENT FELL WHEN BEING TRANSFERRED WITH A LIKORALL OVERHEAD LIFT. THE PATIENT WENT TO THE HOSPITAL AND RECEIVED 30 SUTURES TO THE RIGHT SIDE OF THEIR HEAD. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Fall; Head Injury

  MAUDE report 21603712 ↗
• MalfunctionJan 9, 2025Break; Break

  IT WAS REPORTED THAT WHEN A PATIENT WAS BEING MOVED FROM THE BED WITH A LIKORALL 242 LIFT, THE ¿SUSPENSION EYELET ON THE LIFTING JUMPER BROKE¿ CAUSING THE PATIENT TO FALL. THE CUSTOMER REPORTED ¿LIGHTER PHYSICAL INJURIES¿ BECAUSE THE PATIENT LANDED ON THE BED, BUT THE FALL CAUSED FEARS. THE LOCAL BAXTER TEAM IN SWEDEN OBTAINED THE FOLLOWING ADDITIONAL INFORMATION. THE FEMALE PATIENT WAS REPORTED TO BE BETWEEN 65-85 YEARS OLD AND WEIGHED 46-90 KG. AT THE TIME OF THE REPORTED INCIDENT, THE LIKORALL 242 WAS BEING USED WITH A UNIVERSAL SLINGBAR 450 (PROD. NO. 3156085) AND A GULDMANN BASIC BASIC L SLING. THE COMPOSITE HOOK ON THE UNIVERSAL SLINGBAR BROKE WHEN THE PATIENT WAS RAISED 20 CM ABOVE THE BED AND THE PATIENT¿S FOREHEAD HIT THE SIDERAIL OF THE BED. THE NURSE ASSESSED THE PATIENT¿S VITAL SIGNS AND SKIN STATUS, AND NO TREATMENT WAS REQUIRED.

  Patient problems: Fall

  MAUDE report 21110061 ↗
• MalfunctionNov 20, 2024Break; Break

  A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 242 S, COMPOSITE HOOK BROKE DURING A 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 20736550 ↗
• MalfunctionOct 2, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER ALLEGED THE LIFT¿S MOTOR WAS NONFUNCTIONAL AFTER A BATTERY CHANGE THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20350886 ↗
• MalfunctionFeb 7, 2023Fracture; Fracture

  IT WAS REPORTED THAT ONE OF THE SLINGBAR'S HOOKS BROKE DURING A PATIENT TRANSFER. THERE WAS NO PATIENT/CAREGIVER INJURY REPORTED AS THE PATIENT FELL BACK ONTO THE BED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16311823 ↗