MAUDE Adverse Event Report: ETAC A/S MOLIFT; QUICK RAISER 205

Model Number	QUICK RAISER 205
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Unspecified Skin and Subcutaneous Tissue Problem (4927)
Date of Event	06/06/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Several attempts both via email and phone were made by the importer to gather additional information.No response was given by end user.Should additional information be given a supplemental report will be prepared and submitted.
Event or Problem Description
Hovertech received information regarding an incident in which an individual sustained a laceration to the knee while being transferred to a standing position using the molift quick raiser 205.According to the information received, the lifting arm was moving upward during the transfer when the injury occurred.The injury required several sutures for closure.Moreover, it was reported that there does not appear to be any equipment failure.

• Brand Name: MOLIFT
• Common Device Name: QUICK RAISER 205
• Manufacturer (Section D): ETAC A/S; parallelvej 3; gedved, midtjylland 8751 ; DA 8751
• MDR Report Key: 25725178
• Report Number: 2531468-2026-00001
• Device Sequence Number: 5737943
• Product Code: FSA
• UDI-Device Identifier: 05707995033185
• UDI-Public: 05707995033185
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Importer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 07/06/2026
• Report Date (Section F): 06/12/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Model Number: QUICK RAISER 205
• Device Catalogue Number: 2900000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 06/12/2026
• Device Age: 9 YR
• Event Location: Other
• Date Report to Manufacturer: 06/12/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 07/06/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown