MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DRAPE,U/ SHT,SPLIT,PLASTIC,ST,1EA

Catalog Number	DYNJP2499H
Medical Device Problem Codes	Material Puncture/Hole (1504); Material Split, Cut or Torn (4008)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/19/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Customer receieved 1ea opened the package damaged; the inside cover is ripped, bu the outside plastic was intact.No sample was received; one picture was received and the photo shows two small holes in the drape.The issue was confirmed, but medline was unable to determine the root cause.Complaint history and nonconformance trending for this product and this customer for the past six months were reviewed, and medline will monitor for 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.
Event or Problem Description
It was reported that customer receieved 1ea of dynjp2499 opened the package damaged.The inside cover is ripped, bu the outside plastic was intact.

• Brand Name: MEDLINE
• Common Device Name: DRAPE,U/ SHT,SPLIT,PLASTIC,ST,1EA
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: abdul khan ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50934899
• Report Number: 1417592-2026-53424
• Device Sequence Number: 21231985
• Product Code: PUI
• UDI-Device Identifier: 10080196739462
• UDI-Public: 10080196739462
• Combination Product (Y/N): N
• Initial Reporter State: WA
• 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): 09/29/2026

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: DYNJP2499H
• 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: 10/19/2023
• Initial Report FDA Received Date: 09/29/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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