MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP MEDLINE; TRANSPORT CHAIR, KNOCKDOWN, STEEL

Catalog Number	MDS808200KD
Medical Device Problem Code	Connection Problem (2900)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/31/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was reported that "one of the screws on the transport fell out and is now lost", "it is the hand screw that holds the front right wheel on", "she trying to put the unit in the car when the wheel fell off".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 "she trying to put the unit in the car when the wheel fell off".

• Brand Name: MEDLINE
• Common Device Name: TRANSPORT CHAIR, KNOCKDOWN, STEEL
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093 2753
• Manufacturer Contact: mohammed haider ; three lakes drive; northfield, IL 60093-2753
• MDR Report Key: 25540673
• Report Number: 1417592-2026-02670
• Device Sequence Number: 18481300
• Product Code: INM
• UDI-Device Identifier: 00888277329983
• UDI-Public: 00888277329983
• Combination Product (Y/N): N
• Initial Reporter State: SC
• 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: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 06/17/2026

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: MDS808200KD
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/31/2026
• Initial Report FDA Received Date: 06/17/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/01/2024
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown