MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; PAD,NON-STICK,CURAD,W/ADH,2X3,ST,20/BX

Catalog Number	CUR47147RB
Medical Device Problem Codes	Loss of or Failure to Bond (1068); Material Split, Cut or Torn (4008)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/30/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "pads are falling apart and adhesive tabs don't stick".
Additional Manufacturer Narrative
The customer reported that the pads were falling apart and adhesive tabs don't stick.Physical samples were reviewed; from the box, 3 ea were opened and reviewed, and each product visually inspected was within specification.Based on the review of the samples, medline was unable to confirm the reported issue that the pads were falling apart and that there were issues with the adhesives; no root cause was identified, and medline cannot confirm the issue is manufacturing related.The divisional quality representative will continue to monitor this issue for tracking and trending purposes during quarterly trending.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: PAD,NON-STICK,CURAD,W/ADH,2X3,ST,20/BX
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: koushik pothamshetty ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50778500
• Report Number: 1417592-2026-41355
• Device Sequence Number: 10664006
• Product Code: NAB
• UDI-Device Identifier: 00080196300023
• UDI-Public: 00080196300023
• Combination Product (Y/N): N
• Initial Reporter State: FL
• 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): 09/14/2026

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: CUR47147RB
• 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: 04/30/2024
• Initial Report FDA Received Date: 09/15/2026
• 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: Male