Likorall™ overhead lift 3124050Recalls & reported problems

Summary

The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 00887761979567), received between Aug 15, 2021 and Jun 10, 2026 — classified as 18 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (12 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 18 most recent of 18 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• 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 ↗
• MalfunctionSep 9, 2025Mechanical Problem; Mechanical Problem

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 250 S, NATURAL, IRC,HAD AN ISSUE, EMERGENCY BUTTON DAMAGED. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. 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 23004536 ↗
• MalfunctionApr 25, 2025Mechanical Problem; Mechanical Problem

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 250 S, NATURAL, IRC EMERGENCY STOP DOES NOT WORK IF IT IS PUSHED. 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 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 21908275 ↗
• MalfunctionFeb 19, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, 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 21410998 ↗
• MalfunctionFeb 11, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, 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 21353718 ↗
• MalfunctionFeb 4, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, IRC WAS MISSING EMERGENCY STOP CORD. 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 21303874 ↗
• MalfunctionJan 9, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, IRC 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 21111862 ↗
• MalfunctionDec 12, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, IRC EMERGENCY PULL 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 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 20912552 ↗
• MalfunctionDec 3, 2024Mechanical Problem; Mechanical Problem

  THE CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 250 PATIENT LIFT EMERGENCY STOP WAS NOT ENGAGING.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 20831476 ↗
• MalfunctionDec 3, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT THE LIKORALL 250 PATIENT LIFT 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 20830396 ↗
• MalfunctionNov 4, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 S, NATURAL, IRC HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK IT WAS NOTED THAT THE EMERGENCY PULL 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 20600453 ↗
• MalfunctionOct 22, 2024Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT THE LIKORALL 250 PATIENT LIFT EMERGENCY STOP BUTTON DOES NOT WORK. LIFT CAN STILL BE USED WHEN PRESSED. 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 20505358 ↗
• MalfunctionOct 22, 2024Mechanical Problem; Mechanical Problem

  A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE LIKORALL 250 LIFT, HAD AN ISSUE, THE EMERGENCY PULL 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 20505339 ↗
• MalfunctionOct 17, 2024Incomplete or Missing Packaging; Incomplete or Missing Packaging

  DURING SERVICING BY BAXTER, IT WAS IDENTIFIED THAT THE LIKORALL 250 PATIENT LIFT HAD A MISSING EMERGENCY STOP CORD. 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 BAXTER TECHNICIAN REPLACED THE EMERGENCY STOP CORD TO RESOLVE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20472093 ↗
• MalfunctionMay 12, 2022Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working

  THE CUSTOMER REPORTED HAVING ISSUES WITH THE LIFT¿S EMERGENCY STOP BUTTON. IN THE SPECIFIC, WHEN TESTING THE UNIT WITH 450 LBS WEIGHT TEST AND PULLING THE EMERGENCY STOP BUTTON, THE LIFT STILL LOWERS WHEN PRESSING THE DOWN BUTTON. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14367871 ↗
• MalfunctionAug 15, 2021Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE LIFT WAS LOWERING EVEN THOUGH THE EMERGENCY STOP BUTTON WAS PRESSED. THE LIFT WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12322475 ↗