MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; TRANS CHAIR, 22", RDLA,SA, NYLON, 450 LB

Catalog Number	TCB228N21S
Medical Device Problem Code	Activation Problem (4042)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/25/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "the right side legrest is no locking staying in the elevated position and will just fall.".
Additional Manufacturer Narrative
Per customer call, the transport chair arrived less than a month ago, and the right side legrest is no locking staying in the elevated position and will just fall; no fall or injury was reported during this phone.Sample and/or photo/video was not available, medline quality followed up with the customer to try and obtain the necessary information, pcn history was reviewed, and quality control inspection records were reviewed.Investigation results were not confirmed.No product changes were identified that could have contributed to the alleged product failure, and a formal investigation will be conducted should the customer provide medline quality with a photo, video, or a physical sample.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.This medical device report (mdr) is being submitted as part of retrospective review activities, which include review of historical data in accordance with regulations at 21 cfr part 803.The information included in this mdr reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.

• Brand Name: MEDLINE
• Common Device Name: TRANS CHAIR, 22", RDLA,SA, NYLON, 450 LB
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: ankitha komirishetty ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50868046
• Report Number: 1417592-2026-48672
• Device Sequence Number: 13067227
• Product Code: INM
• UDI-Device Identifier: 00193489036810
• UDI-Public: 00193489036810
• Combination Product (Y/N): N
• Initial Reporter State: NH
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/22/2026

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: TCB228N21S
• Device Lot Number: 16424040002
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/25/2024
• Initial Report FDA Received Date: 09/23/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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
• Patient Sequence Number: 1
• Patient Sex: Unknown