MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION LIKO M230 MOBILE LIFT; LIFT PATIENT NON AC POWERED

Model Number	2050015
Medical Device Problem Code	Device Fell (4014)
Health Effect - Clinical Code	Fall (1848)
Date of Event	12/21/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Upon inspection, the baxter technician found the actuator needed to be replaced.Liko m220 and m230 mobile lifts are easy-to-use mobile lifts primarily intended for use in nursing homes.Both models are excellent aids for daily transfers of adults and children; for instance, for transfers to and from a wheelchair, toilet and floor.The models differ in the way the base width is adjusted while both lifts feature an electric lift mechanism.Liko m230 mobile lift has an electric base and liko m220 mobile lift a manual base for opening and closing the legs.The baxter technician replaced the actuator to resolve.Based on this information, no further action is required.Although there was no reported injury with this event, if a patient fall during transfer were to recur, it could potentially cause serious injury or death.Therefore baxter is reporting this event.
Event or Problem Description
On 30-dec-2025, a customer contacted technical service to report that liko m230 (product code 2050015, serial number (b)(6)), had patient being transferred from a wheelchair to a bed using a personal lift when the battery ran out and made patient fall onto the bed.This occurred during patient use.There was no patient/user injury, medical intervention, symptom, or adverse event reported.There were no other devices reported to be involved.

• Brand Name: LIKO M230 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 ; 2242702068
• MDR Report Key: 24168396
• Report Number: 8030916-2026-00009
• Device Sequence Number: 18399305
• Product Code: FSA
• UDI-Device Identifier: 00887761981904
• UDI-Public: (01)00887761981904(11)250818
• Combination Product (Y/N): N
• Initial Reporter Country: FI
• 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): 01/23/2026

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: 2050015
• Device Catalogue Number: 2050015
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/19/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/30/2025
• Initial Report FDA Received Date: 01/23/2026
• 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 Age: 60 YR
• Patient Sex: Unknown
• Patient Weight: 70 KG