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

Model Number	2040045
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/15/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Upon inspection, the technician found the emergency stop button needed to be replaced.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.The technician replaced the emergency stop button to resolve the reported issue.A report of a emergency function not working in an operative lift is likely to cause or contribute to a death or serious injury.
Event or Problem Description
A other health care professional contacted technical service to report that viking m lift had an issue, unit emergency button not working.The process step during which this occurred was unknown.There was no patient/user injury, medical intervention, symptom, or adverse event reported.The device was requested for service/inspection by baxter.

• Brand Name: VIKING M
• 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 ; 2242702068
• MDR Report Key: 24038311
• Report Number: 8030916-2026-00005
• Device Sequence Number: 13076470
• Product Code: FSA
• UDI-Device Identifier: 00887761981874
• UDI-Public: (01)00887761981874
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 01/12/2026

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
• Device Model Number: 2040045
• Device Catalogue Number: 2040045
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/16/2025
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/15/2025
• Initial Report FDA Received Date: 01/12/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown