MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DBD-C-SECTION PACK

Catalog Number	DYNJ23544F
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/12/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was reported that ¿i was in or 2 after a case was finished.I still had my sterile gown and gloves on, i leaned against the patient who had some blood on the pad that was tucked under her.The blood went through my gown on my scrubs.The gown was supposed to be impervious but was not.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 "the blood went through my gown on my scrubs.The gown was supposed to be impervious but was not.".

• Brand Name: MEDLINE
• Common Device Name: DBD-C-SECTION PACK
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: camilla allen ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50275707
• Report Number: 1417592-2026-17906
• Device Sequence Number: 10329341
• Product Code: OHM
• UDI-Device Identifier: 40889942533054
• UDI-Public: 40889942533054
• Combination Product (Y/N): N
• Initial Reporter State: MS
• 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): 08/14/2026

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: DYNJ23544F
• Device Lot Number: 23CMD242
• 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: 07/12/2023
• Initial Report FDA Received Date: 08/17/2026
• 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
• Patient Sequence Number: 1
• Patient Sex: Unknown