FDA Adverse Event Malfunction Summary report: N

LIKORALL OVERHEAD LIFT

MDR report key: 24681057 · Received March 24, 2026

Report

Report Number
8030916-2026-00031
Event Type
Malfunction
Date Received
March 24, 2026
Date of Event
February 26, 2026
Report Date
March 24, 2026
Manufacturer
BAXTER HEALTHCARE CORPORATION
Product Code
FSA
UDI-DI
00887761981911
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE BAXTER TECHNICIAN FOUND THE HOOK IS BROKEN AND NEEDED TO BE REPLACED. 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. A SEARCH OF THE BAXTER MAINTENANCE RECORDS SHOWED BAXTER PERFORMED PREVENTATIVE MAINTENANCE ON THIS DEVICE IN MAR 22, 2017. IT IS UNKNOWN IF THE FACILITY PERFORMED ANY OTHER PREVENTATIVE MAINTENANCE ON THIS DEVICE. THE TECHNICIAN REPLACED THE LIFT BAR TO RESOLVE THE REPORTED EVENT. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

Description of Event or Problem · 0

ON 26-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT LIKORALL 200 (PRODUCT CODE 3121001, SERIAL NUMBER (B)(6)), ONE HOOK ON THE SLINGBAR BREAKS. THE PATIENT FALLS DOWN ON THE BED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
741557 LIKORALL OVERHEAD LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 3121001 00887761981911

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown