MAUDE Adverse Event Report: SAVARIA LIFTS (UK) LTD. SAVARIA LIFTS (UK) LTD.; STAIRLIFT

Model Number	2000
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/21/2026
Type of Reportable Event	Malfunction
Event or Problem Description
End user was riding the stairlift upward, when they heard a pop.They safely rode to the nearest stop at the bottom and it was found that the rail had a small break.They rode over the weld break and safely exited the stairlift without any injury.

• Brand Name: SAVARIA LIFTS (UK) LTD.
• Common Device Name: STAIRLIFT
• Manufacturer (Section D): SAVARIA LIFTS (UK) LTD.; 82 first avenue; pensnett estate; kingswinford, west midlands DY6 7 FJ; UK DY6 7FJ
• MDR Report Key: 25255824
• Report Number: 3005753836-2026-00003
• Device Sequence Number: 5496099
• Product Code: PCD
• UDI-Device Identifier: 05056233700045
• UDI-Public: 5056233700045
• Combination Product (Y/N): N
• Initial Reporter State: TX
• 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: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/21/2026
• Report Date (Section F): 05/21/2026

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: 2000
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 04/24/2026
• Device Age: 5 YR
• Event Location: Home
• Date Report to Manufacturer: 05/21/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/22/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown