MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; REGULATOR,SUCTION,CONT/INT,DISS BTM,CHEM

Catalog Number	RTACIDCM
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/30/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that back mounting plate lower bottom potion spiket.Bottom plastic spreader piece not working/damed.
Additional Manufacturer Narrative
A quality complaint was received for one unit where it was stated that the bottom plastic spreader piece is not working/damaged.Medline visually inspected the sample and can see the plastic on the bottom of the unit is cracked, and performed a retrospective query on the item number for the past six months and found no similar complaints.As a result, medline confirmed the issue.Vendor review determined the canister was hung off the suction regulator at an angle, causing excess weight on the patient port and resulting in damage; the division will monitor for trends.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: REGULATOR,SUCTION,CONT/INT,DISS BTM,CHEM
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: shravan ingole ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50856495
• Report Number: 1417592-2026-47900
• Device Sequence Number: 13138746
• Product Code: KDP
• UDI-Device Identifier: 10193489014334
• UDI-Public: 10193489014334
• Combination Product (Y/N): N
• Initial Reporter State: NY
• 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: RTACIDCM
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 02/17/2023
• 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: 01/30/2023
• 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): 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