MAUDE Adverse Event Report: FERNO-WASHINGTON, INC. TRANSCEND CHAIR W/TRX

Model Number	0731402
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/08/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was found during an inspection of the chair that one of the transport wheels had detached from the chair.There was no report of patient involvement or adverse event associated with the reported issue.The issue was confirmed via conversation with technical support and replacement parts were provided for the repair.The customer confirmed the repair was completed and the chair was returned to service.

• Brand Name: TRANSCEND CHAIR W/TRX
• Common Device Name: TRANSCEND CHAIR W/TRX
• Manufacturer (Section D): FERNO-WASHINGTON, INC.; 70 wiel way; wilmington OH 45177
• Manufacturer (Section G): FERNO-WASHINGTON, INC.; 70 wiel way; wilmington OH 45177
• Manufacturer Contact: dawn greene ; 70 wiel way; wilmington, OH 45177 ; 9372832900
• MDR Report Key: 22157795
• Report Number: 1523574-2025-00056
• Device Sequence Number: 20709348
• Product Code: FPP
• UDI-Device Identifier: 00190790004057
• UDI-Public: (01)00190790004057(11)230823(
• Combination Product (Y/N): N
• Initial Reporter State: UT
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 06/06/2025

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: Health Professional
• Device Model Number: 0731402
• Device Catalogue Number: 0731402
• Device Lot Number: M669790
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/08/2025
• Initial Report FDA Received Date: 06/06/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/23/2023
• 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 Sex: Unknown