MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP MEDLINE; TRAP,MUCUS, 10FR, DELEE, W/VALVE

Catalog Number	DYND44110
Medical Device Problem Codes	Suction Problem (2170); Suction Failure (4039)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	02/23/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
According to the customer, "the suction catheter did not work when needed for infant resuscitation.Multiple suction catheters have to be used when these don't provide suction." no additional information at this time.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
Event or Problem Description
According to the customer, "the suction catheter did not work when needed for infant resuscitation.Multiple suction catheters have to be used when these don't provide suction.".

• Brand Name: MEDLINE
• Common Device Name: TRAP,MUCUS, 10FR, DELEE, W/VALVE
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; 3 lakes dr; northfield IL 60093
• Manufacturer Contact: alyssa reasner ; 3 lakes dr; northfield, IL 60093
• MDR Report Key: 23908513
• Report Number: 1417592-2025-00748
• Device Sequence Number: 9925129
• Product Code: BYZ
• UDI-Device Identifier: 10080196997404
• UDI-Public: 10080196997404
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 12/29/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: DYND44110
• Device Lot Number: 18322120001
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/01/2025
• Initial Report FDA Received Date: 12/29/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other; Required Intervention
• Patient Sex: Unknown