MAUDE Adverse Event Report: CENTURION MEDICAL PRODUCTS CORPORATION Centurion; DRESSING, SURESITE SELECT, 2.75"X2 7/8"

Catalog Number	VAD1683
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	09/08/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The account reported finding dressing not sticking; the complaint also states the suresite dressing was not adhering properly and had peeled off of patients.A sample was received for the investigation; 3 ea were received and 20 ea were pulled from inventory, and the samples returned and the samples from inventory had visual presence of the adhesive and passed functional testing by application and removal from a test surface.Finished good production records and finished good pack build were reviewed, with no run without approvals, deviations or non-conformance reports and no issues with the build that likely contributed to the reported issue.No defects were identified; per the complaint details and sample received, the reported issue was unable to be confirmed, the root cause cannot be determined, and this issue will be monitored by centurions complaint system.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.
Event or Problem Description
It was reported that "we have been getting complaints about the suresite dressing vad1683 not sticking properly." it was also reported that "it has peeled off of patients.".

• Brand Name: Centurion
• Common Device Name: DRESSING, SURESITE SELECT, 2.75"X2 7/8"
• Manufacturer (Section D): CENTURION MEDICAL PRODUCTS CORPORATION; 100 centurion way; williamston MI 48895
• Manufacturer Contact: azra halilovic ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50870173
• Report Number: 1417592-2026-49016
• Device Sequence Number: 9223577
• Product Code: KMK
• UDI-Device Identifier: 00653160329018
• UDI-Public: 00653160329018
• Combination Product (Y/N): N
• Initial Reporter State: MO
• 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: VAD1683
• Device Lot Number: 2023052601
• 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: 09/08/2023
• Initial Report FDA Received Date: 09/23/2026
• 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): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown