MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; BANDAGE,PLASTC,CURAD,60CT,3/4X3"

Catalog Number	CUR45153RB
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	07/08/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "they do not stick at all" and "no luck.No stick.".
Additional Manufacturer Narrative
A complaint was received regarding weak adhesion from plastic bandages; the customer reported that the bandages ¿do not stick at all¿ and ¿no luck.No stick.¿ the provided samples were evaluated, the coa for the product lot was requested from the vendor, and trend analysis was performed by reviewing the past two years of complaint data.The bandages were visually inspected for visual defects, none were noted, and the bandages were able to adhere to a clean, dry surface without signs of weak adhesion; the reported issue could not be identified or replicated.Based on the information provided and the results of the investigation, medline was not able to confirm the reported issue or that the product failed to meet specifications; the cause was not confirmed with received 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: BANDAGE,PLASTC,CURAD,60CT,3/4X3"
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: felipe bifareti
• MDR Report Key: 50716708
• Report Number: 1417592-2026-36003
• Device Sequence Number: 16111287
• Product Code: KGX
• UDI-Device Identifier: 00080196302850
• UDI-Public: 00080196302850
• Combination Product (Y/N): N
• Initial Reporter State: OK
• 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): 09/06/2026

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: CUR45153RB
• Device Lot Number: 90924050001
• 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: 07/08/2025
• Initial Report FDA Received Date: 09/10/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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