MAUDE Adverse Event Report: BEKA Hospitec BEKA Hospitec; Lift, Patient, Non-Ac-Powered

Model Number	920108000
Medical Device Problem Codes	Failure to Cycle (1142); Mechanical Jam (2983)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/21/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
A resident became stuck in an elevated position because the lift would not lower, even after attempting to use the emergency lowering function.

• Brand Name: BEKA Hospitec
• Common Device Name: Lift, Patient, Non-Ac-Powered
• Manufacturer (Section D): BEKA Hospitec; am rübenmorgen 3; wetzlar, hessen 35582 ; GM 35582
• MDR Report Key: 50354358
• Report Number: 3007802293-2026-00005
• Device Sequence Number: 14962464
• Product Code: FSA
• UDI-Device Identifier: 04260735020025
• UDI-Public: 04260735020025
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/18/2026
• Report Date (Section F): 08/18/2026

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: 920108000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 07/22/2026
• Event Location: Other
• Date Report to Manufacturer: 08/05/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/20/2026
• 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