Likorall™ overhead lift 3122502Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00887761979505), received between Aug 5, 2022 and May 7, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Fracture” (2 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• MalfunctionJul 8, 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 250 ES, WHITE HAD AN ISSUE, THE SAFETY CABLE DID NOT GET STUCK WHEN A PATIENT FELL. 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 22437687 ↗
• MalfunctionFeb 5, 2025Mechanical Problem; Mechanical Problem

  DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 250 ES, WHITE HAD AN ISSUE, WHILE PERFORMING FUNCTIONS CHECK NOTICED EMERGENCY STOP ACTIVATOR CORD WAS 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 21311161 ↗
• MalfunctionOct 4, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER ALLEGED THE PATIENT WAS ON A LIFT AND THE LIFT RAIL PULLED OUT FROM THE CEILING CAUSING THE PATIENT TO BE DROPPED BACK INTO THE CHAIR. THERE WAS NO ALLEGATION OF PATIENT OR CAREGIVER INJURY OR DEATH REPORTED FROM THIS ALLEGED INCIDENT. THIS INCIDENT WAS CAPTURED UNDER COMPLAINT REF#: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20370069 ↗
• MalfunctionAug 5, 2022Fracture; Fracture

  THE CUSTOMER REPORTED THAT WHILE ATTEMPTING TO MOVE A PATIENT USING THE LIKORALL 250 DEVICE, THE DEVICE'S SLING BAR COMPOSITE HOOK BROKE OFF THE SLING BAR. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15173184 ↗