MAUDE Adverse Event Report: SAVARIA LIFTS (UK) SAVRAIA LIFTS (UK) LTD - HANDICARE; CURVED STAIRLIFT

Model Number	2000
Medical Device Problem Codes	Vibration (1674); Failure to Align (2522)
Health Effect - Clinical Code	Bruise/Contusion (1754)
Date of Event	02/20/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
End user states that seat swivel did not work.End user travelled up stairs, once at the landing the swivel motor failed to engage.End user attempted to leave the lift in a panicked state, upon disembarking his legs gave way resulting in him falling against the wall and being unable to get up.Sustained bruises.
Additional Manufacturer Narrative
Swivel motor failure, issue resolved.Incident attributable to end users panic and pre-existing medical condition which caused end users legs to give way when dismounting, resulting in end user leaving the chair in an unsafe manner.Initial report of incident did not cover injuries sustained by end user, upon further information incident was determined to be reportable.

• Brand Name: SAVRAIA LIFTS (UK) LTD - HANDICARE
• Common Device Name: CURVED STAIRLIFT
• Manufacturer (Section D): SAVARIA LIFTS (UK); 82 first avenue; pensnett estate; kingswinford, west midlands DY6 7 FJ; UK DY6 7FJ
• Manufacturer (Section G): SAVARIA LIFTS (UK) LTD; 82 first avenue; pensnett estate; kingswinford, west midlands DY6 7 FJ; UK DY6 7FJ
• Manufacturer Contact: duncan walker ; 82 first avenue; pensnett estate; kingswinford, west midlands DY6 7-FJ ; UK DY6 7FJ
• MDR Report Key: 24982057
• Report Number: 3011268530-2026-00003
• Device Sequence Number: 10514999
• Product Code: PCD
• UDI-Device Identifier: 05056233700045
• UDI-Public: (01)05056233700045(11)200227
• 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: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Remedial Action: Replace
• Type of Report: Initial
• Report Date (Section B): 04/21/2026

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
• Operator of Device: Lay User/Patient
• Device Model Number: 2000
• Device Catalogue Number: ST00575468
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/17/2026
• Initial Report FDA Received Date: 04/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/27/2020
• 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: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization
• Patient Sex: Male