MAUDE Adverse Event Report: Medline ReNewal MEDLINE CO-LABEL; BW CATH CABL THERMCOOL 34PN BLK-34PN RED

Catalog Number	CR3434CTRH
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/26/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "bad cable broken pin.".
Additional Manufacturer Narrative
The reported issue was noted as "bad cable broken pin." the investigation included review of the original manufacturing records and evaluation of the device, including visual inspection; no observations were noted during the record review and the device passed all approved testing and inspections.Upon visual inspection, a bent pin was identified in the connector of the cable, and no other damage or defects were identified.The cause was identified as misuse/mishandling, traced to user, and medline renewal trends and monitors all complaints to ensure no systemic issues exist.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 CO-LABEL
• Common Device Name: BW CATH CABL THERMCOOL 34PN BLK-34PN RED
• Manufacturer (Section D): Medline ReNewal; 1500 ne hemlock avenue; redmond OR 94456 -187
• Manufacturer Contact: brianna montgomery ; three lakes drive; northfield, IL 60093
• MDR Report Key: 50889568
• Report Number: 3032391-2026-00177
• Device Sequence Number: 9791558
• Product Code: IKD
• UDI-Device Identifier: 10197344014163
• UDI-Public: 10197344014163
• Combination Product (Y/N): N
• Initial Reporter State: CA
• 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): 09/24/2026

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: CR3434CTRH
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 05/26/2023
• 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: 05/26/2023
• Initial Report FDA Received Date: 09/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): Yes
• Patient Sequence Number: 1
• Patient Sex: Unknown