MAUDE Adverse Event Report: FERNO Transcend Stair Chair w/Trx

Model Number	0731402
Medical Device Problem Code	Unintended Movement (3026)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction

• Brand Name: Transcend Stair Chair w/Trx
• Common Device Name: Transcend Stair Chair w/Trx
• Manufacturer (Section D): FERNO; 70 weil way; wilmington OH 45177
• Manufacturer (Section G): FERNO; 70 weil way; wilmington OH 45177
• Manufacturer Contact: dawn greene ; 70 weil way; wilmington, OH 45177 ; +1(937)283-2900
• MDR Report Key: 50168261
• Report Number: 1523574-2026-00084
• Device Sequence Number: 5252795
• Product Code: FPP
• UDI-Device Identifier: 00190790004057
• UDI-Public: (01)00190790004057(11)260211
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 08/06/2026

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: Health Professional
• Device Model Number: 0731402
• Device Catalogue Number: 0731402
• Device Lot Number: M252400
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/08/2026
• Initial Report FDA Received Date: 08/06/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/19/2026
• 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