MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; LINER,SOFT,SUCTION CANISTER,1500CC

Catalog Number	DYNDSCL1500
Medical Device Problem Code	Difficult to Open or Close (2921)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/10/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "item wasn't working.They weren't closing".
Additional Manufacturer Narrative
The reported issue was "item not closing", and the complaint transcript stated, "item wasn't working.They weren't closing".Medline quality received 1 cs of the item for evaluation; visual inspection of the provided product revealed no defects nor abnormalities, and functional testing was conducted by connecting the product to a vacuum and observing whether it suctioned liquid as intended.Functional testing of the product revealed no defects nor abnormalities, and the reported concern could not be confirmed, as the sample functioned normally; the cause was documented as "not confirmed with received sample".The division will continue to monitor this issue 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.

• Brand Name: MEDLINE
• Common Device Name: LINER,SOFT,SUCTION CANISTER,1500CC
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: azmat shah ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50855189
• Report Number: 1417592-2026-47661
• Device Sequence Number: 9652018
• Product Code: KDQ
• UDI-Device Identifier: 40884389129532
• UDI-Public: 40884389129532
• 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): 09/21/2026

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: DYNDSCL1500
• Device Lot Number: 670231006
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 04/23/2024
• 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: 04/10/2024
• Initial Report FDA Received Date: 09/22/2026
• 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
• Patient Sequence Number: 1
• Patient Sex: Unknown