MAUDE Adverse Event Report: MEDLINE INDUSTRIES LP MEDLINE; WHLCHAIR, K3, 20", SB DDLA, SA FOOT

Catalog Number	K3206N24S
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/25/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was reported that the "patient states that she heard and felt a pop when sitting down into the chair then noticed the left rear wheel pinned against the left armrest assembly.Patient stated they got out of the wheelchair because the left wheel wouldn't roll due to it being pinned against the left armrest assembly." there were no reports of death, serious injury, medical intervention, or follow up care.It has been determined that the reported event could cause or contribute to serious injury if it were to occur again.In an abundance of caution, this is a reportable event.If additional information becomes available this report will be reopened and reevaluated.
Event or Problem Description
It was reported that the customer "heard and felt a pop when sitting down into the chair then noticed the left rear wheel pinned against the left armrest assembly.".

• Brand Name: MEDLINE
• Common Device Name: WHLCHAIR, K3, 20", SB DDLA, SA FOOT
• Manufacturer (Section D): MEDLINE INDUSTRIES LP; three lakes drive; northfield IL 60093 2753
• Manufacturer Contact: jeffrey johnson ; three lakes drive; northfield, IL 60093-2753
• MDR Report Key: 25100585
• Report Number: 1417592-2026-00816
• Device Sequence Number: 9959852
• Product Code: IOR
• UDI-Device Identifier: 00193489087164
• UDI-Public: 00193489087164
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• PMA/510(K) Number: K990463
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 05/06/2026

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
• Device Catalogue Number: K3206N24S
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/06/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 11/01/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Age: 49 YR
• Patient Sex: Female
• Patient Weight: 113 KG
• Patient Race: White