FDA Adverse Event Malfunction Summary report: N

LIKORALL 200

MDR report key: 23450189 · Received November 3, 2025

Report

Report Number
8030916-2025-00127
Event Type
Malfunction
Date Received
November 3, 2025
Date of Event
October 8, 2025
Report Date
November 3, 2025
Manufacturer
BAXTER HEALTHCARE CORPORATION
Product Code
FSA
UDI-DI
00887761981911
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE BAXTER TECHNICIAN REPLACED THE EMERGENCY STOP BUTTON. LIKORALL OVERHEAD LIFT IS A STATIONARY LIFT MOUNTED IN A RAIL SYSTEM. THE RAIL SYSTEM CAN BE BUILT STRAIGHT, WITH OR WITHOUT CURVES, AS A TRAVERSE SYSTEM AND ALSO AS A ROOM-TO-ROOM SYSTEM. LIKORALL OVERHEAD LIFT IS INTENDED FOR USE IN LIFTING AND TRANSFERRING PATIENTS, FOR EXAMPLE, FROM BED TO A WHEELCHAIR, TO OR FROM THE FLOOR, FOR VISITS TO THE TOILET, FOR GAIT, STANDING AND BALANCE TRAINING, WHEN WEIGHING THE PATIENT AND WHEN LIFTING THE PATIENT WITH A STRETCHER. ALTHOUGH THERE WAS NO ADVERSE EVENT REPORTED, A REPORT OF A EMERGENCY STOP FUNCTION NOT WORKING IN AN OPERATIVE LIFT IS LIKELY TO CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY.

Description of Event or Problem · 0

DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT LIKORALL 200 HAD AN ISSUE, EMERGENCY STOP NOT FUNCTIONING. 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.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1798194 LIKORALL 200 LIFT PATIENT NON AC POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 NA 00887761981911

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown N/A.