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

Model Number	185090
Medical Device Problem Codes	Break (1069); Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	Laceration(s) (1946)
Date of Event	03/29/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The customer reported that a patient fell during a routine transfer from a bed to a chair using a viking m mobile lift.The sling was applied to the patient and the lift was operated by two care staff.While the patient was suspended and being moved toward the chair, staff reported hearing a crackling noise, followed immediately by the sling bar detaching from the lift while the patient was positioned midway through the transfer in the center of the room.The registered nurse in charge and care staff immediately attended to the patient.The customer reported active bleeding from the back of the patient¿s head, which was managed by applying pressure.Paramedics were called and arrived on site, provided first aid, and assisted in returning the patient safely to bed using a different lift device.Paramedics advised continued monitoring and administration of pain relief and indicated that hospitalization was not required at that time.The customer reported that the patient remained stable and that no additional medical intervention was required.The customer also reported that a red plastic component from the quick release hook was found on the floor following the event.No further information was available at the time of this report.
Additional Manufacturer Narrative
Should additional relevant information become available, a supplemental report will be submitted.

• 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: 25020258
• Report Number: 8030916-2026-00053
• Device Sequence Number: 13345451
• 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,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/17/2026

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: Health Professional
• Device Model Number: 185090
• Device Catalogue Number: 185090
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/01/2026
• Supplement Date Received by Manufacturer: 06/26/2026
• Initial Report FDA Received Date: 04/28/2026
• Supplement Report FDA Received Date: 07/17/2026
• 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