MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DBD-TAPE,ELASTIC,FOAM,CURAD,4"X5.5YD,LF

Catalog Number	NON260604Z
Medical Device Problem Code	Loss of or Failure to Bond (1068)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/25/2023
Type of Reportable Event	Malfunction

• Brand Name: MEDLINE
• Common Device Name: DBD-TAPE,ELASTIC,FOAM,CURAD,4"X5.5YD,LF
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: kehkashan khan ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50747795
• Report Number: 1417592-2026-38797
• Device Sequence Number: 13301827
• Product Code: KGX
• UDI-Device Identifier: 00080196765815
• UDI-Public: 00080196765815
• Combination Product (Y/N): N
• Initial Reporter State: WI
• 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): 09/09/2026

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: NON260604Z
• Device Lot Number: 84322092501-H
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 06/12/2023
• 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: 05/25/2023
• Initial Report FDA Received Date: 09/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown