MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DRESSING, CONTACT LAYER, VERSATEL, 2X3

Catalog Number	MSC1723EPZ
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	12/05/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "we are experiencing some issues with the adhesiveness of the versatel dressing.".
Additional Manufacturer Narrative
The customer reported issues with the adhesiveness of the versatel dressing, and the floor was supplementing the adhesive with steri-strips.The reported issue could not be confirmed as no sample was received for investigation, and without a sample a more thorough investigation could not be performed.At this time, medline cannot confirm based off the information received, and the cause was documented as sample required to determine cause.The division will continue to monitor this issue for tracking and trending purposes, and the complaint is ok to close.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: DRESSING, CONTACT LAYER, VERSATEL, 2X3
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: sangameswaran saravanakumar ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50672539
• Report Number: 1417592-2026-33974
• Device Sequence Number: 10235351
• Product Code: NAD
• UDI-Device Identifier: 30884389150980
• UDI-Public: 30884389150980
• Combination Product (Y/N): N
• Initial Reporter State: NY
• 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): 09/03/2026

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: MSC1723EPZ
• Device Lot Number: R15823
• Was Device Available for Evaluation?: Yes
• 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: 12/05/2024
• Initial Report FDA Received Date: 09/08/2026
• Was Device Evaluated by Manufacturer? (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