FDA Adverse Event Malfunction Summary report: N

GOLVO MOBILE LIFT

MDR report key: 24531948 · Received March 6, 2026

Report

Report Number
8030916-2026-00024
Event Type
Malfunction
Date Received
March 6, 2026
Date of Event
February 9, 2026
Report Date
March 6, 2026
Manufacturer
BAXTER HEALTHCARE CORPORATION
Product Code
FSA
UDI-DI
00887761981751
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE BAXTER TECHNICIAN FOUND THE PLATINUM FASTENER WAS LOOSED AND NEEDED TO BE REPLACED. THE GOLVO MOBILE LIFT IN INTENDED TO BE USED FOR TRANSFERRING PATIENTS (ADULT OR CHILDREN) BETWEEN DEVICES (E.G., WITHIN THE ROOM), FLOOR LIFTING, HORIZONTAL LIFTING, SUPPORTING PATIENT LIMBS, AMBULATING PATIENT, BATHING PATIENT, TOILETING PATIENT, WEIGHING PATIENT AND TRANSFERRING PATIENTS FROM CAR. INTENDED FOR USE IN FOLLOWING ENVIRONMENTS: HEALTH CARE, INTENSIVE CARE, EMERGENCY WARD, REHABILITATION, HABILITATION. A SEARCH OF THE BAXTER MAINTENANCE RECORDS DID NOT SHOW BAXTER PERFORMED ANY PREVENTATIVE MAINTENANCE ON THIS DEVICE. IT IS UNKNOWN IF THE FACILITY PERFORMS PREVENTATIVE MAINTENANCE ON THEIR DEVICE. THE TECHNICIAN DISMANTLING THE MAST AND TIGHTENING THE MAST PLATE TO RESOLVE THE REPORTED EVENT. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

Description of Event or Problem · 0

ON 09-FEB-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT GOLVO 9000 LOWBASE (PRODUCT CODE 2000049, SERIAL NUMBER (B)(6)), HAD MAST DAMAGED AND MOVING DURING PATIENT TRANSFER. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
591136 GOLVO MOBILE LIFT LIFT, PATIENT, NON-AC-POWERED FSA BAXTER HEALTHCARE CORPORATION 2000049 00887761981751

Patients

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