MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION VIKING M MOBILE LIFT; LIFT, PATIENT, NON-AC-POWERED

Model Number	P2040005
Medical Device Problem Code	Unstable (1667)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/13/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The baxter technician found the middle bam and plastic inserts needed to be replaced.A search of the baxter maintenance records showed baxter performed preventative maintenance on this device in apr 11, 2025.It is unknown if the facility performed any other preventative maintenance on this device.Viking m mobile lift is a general-purpose lift with the intended use in; health care, intensive care and rehabilitation.Viking m mobile lift is an excellent aid in daily transfers of both adults and children.With 3 various lifting height positions viking m mobile lift gives a flexibility for most lifting situations such as lifting to and from wheel chair, bed, toilet and floor.Horizontal lifting can also be performed in combination with the liko¿ octostretch¿ accessory.The technician replaced the middle bam and plastic inserts to resolve the reported event.Based on this information, no further action is required.
Event or Problem Description
Baxter received a report that viking m, wheel 75/75 had mast tilting forward under load.The process step during which this occurred was unknown.There was no patient/user injury, medical intervention, symptom, or adverse event reported.

• Brand Name: VIKING M MOBILE LIFT
• Common Device Name: LIFT, PATIENT, NON-AC-POWERED
• Manufacturer (Section D): BAXTER HEALTHCARE CORPORATION; deerfield IL
• Manufacturer (Section G): LIKO AB; nedre vagen 100; lulea, norrbottens lan [se-25] 975 9 2; SW 975 92
• Manufacturer Contact: 25212 w. illinois route 120; round lake, IL 60073 ; 2242705355
• MDR Report Key: 25435852
• Report Number: 8030916-2026-00071
• Device Sequence Number: 10284133
• Product Code: FSA
• UDI-Device Identifier: 00887761981874
• UDI-Public: (01)00887761981874
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 06/08/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: P2040005
• Device Catalogue Number: P2040005
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/13/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/13/2026
• Initial Report FDA Received Date: 06/08/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown