Likorall™ overhead lift 3123001Recalls & reported problems

Summary

The FDA's MAUDE database contains 32 adverse event reports that list this exact device (DI 00887761979529), received between Oct 31, 2024 and Jul 2, 2026 — classified as 1 death, 31 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (29 reports).

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.

Recalls naming this device

1. 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

Recent adverse event reports

The 25 most recent of 32 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• MalfunctionFeb 11, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE 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 21353972 ↗
• MalfunctionFeb 11, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE 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 21353853 ↗
• MalfunctionFeb 11, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21353757 ↗
• MalfunctionFeb 11, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21353498 ↗
• MalfunctionFeb 6, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21321157 ↗
• MalfunctionFeb 6, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21320987 ↗
• MalfunctionFeb 5, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21311750 ↗
• MalfunctionFeb 5, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21311381 ↗
• MalfunctionFeb 5, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21311325 ↗
• MalfunctionFeb 4, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21304223 ↗
• MalfunctionFeb 4, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES WHILE PERFORMING FUNCTIONS CHECK NOTICED EMERGENCY STOP CORD WAS MISSING. 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.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21304047 ↗
• MalfunctionJan 27, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21242551 ↗
• MalfunctionJan 27, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21242511 ↗
• MalfunctionJan 27, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ESHAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK NOTICED EMERGENCY GUARD ACTIVATOR MISSING. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21242451 ↗
• MalfunctionJan 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE SLING BAR OF THE LIKORALL 243 LIFT DROPPED DURING A TRANSFER AND MADE CONTACT WITH THE PATIENT CAUSING AN INJURY. IT WAS NOTED THAT THE REPORTER WAS NOT AT LIBERTY TO DISCUSS THE SPECIFIC INJURY THAT RESULTED TO THE PATIENT. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN SPECIFIC DETAILS ABOUT THE REPORTED INJURY AND EVENTUAL MEDICAL/SURGICAL INTERVENTION REQUIRED; HOWEVER, NO ADDITIONAL INFORMATION COULD BE OBTAINED FROM THE CUSTOMER.

  Patient problems: Insufficient Information

  MAUDE report 21195616 ↗
• MalfunctionJan 3, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21068578 ↗
• MalfunctionJan 3, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21068372 ↗
• MalfunctionJan 3, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21068314 ↗
• MalfunctionJan 2, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED DURING TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21060772 ↗
• MalfunctionJan 2, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21060554 ↗
• MalfunctionDec 2, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20820632 ↗
• MalfunctionDec 2, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20819565 ↗
• MalfunctionNov 19, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  BAXTER RECEIVED A USER REPORT FROM THE DANISH MEDICINES AGENCY REPORTING THE FOLLOWING INCIDENT: THE HARNESS WAS NOT TIGHTENED PROPERLY DURING PATIENT USE. THERE WAS NO PATIENT INJURY REPORTED.

  Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

  MAUDE report 20725553 ↗
• MalfunctionNov 14, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 243 ES HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY STOP CORD WAS MISSING. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20681808 ↗