MAUDE Adverse Event Report: TELEFLEX MEDICAL SDN. BHD. BRILLANT 2-W SILICONE FOLEY, TIEMANN; CATHETER, RETENTION TYPE, BALLOON

Model Number	IPN050272
Medical Device Problem Code	Deflation Problem (1149)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/31/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during use on a patient, catheter leaks were found.A bladder scan showed evidence of a high volume of fluid although the catheter was in place.The balloon was tested before use and the inflation volume respected.The lubricant used was optilube.During removal, the balloon was not completely deflated despite the removal of 10ml of sterile water that had been inserted the day before.A presence of deposit on the tip of the urinary catheter was also reported.As a result, the catheter was removed and 3-way catheter was inserted.No harm or injury to the patient.
Additional Manufacturer Narrative
(b)(4).N/a.Other remarks: n/a.Corrected data: n/a.
Additional Manufacturer Narrative
Qn#(b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.Other remarks: n/a.Corrected data: n/a.
Event or Problem Description
It was reported that during use on a patient, catheter leaks were found.A bladder scan showed evidence of a high volume of fluid although the catheter was in place.The balloon was tested before use and the inflation volume respected.The lubricant used was optilube.During removal, the balloon was not completely deflated despite the removal of 10ml of sterile water that had been inserted the day before.A presence of deposit on the tip of the urinary catheter was also reported.As a result, the catheter was removed and 3-way catheter was inserted.No harm or injury to the patient.

• Brand Name: BRILLANT 2-W SILICONE FOLEY, TIEMANN
• Common Device Name: CATHETER, RETENTION TYPE, BALLOON
• Manufacturer (Section D): TELEFLEX MEDICAL SDN. BHD.; perak, west malaysia
• Manufacturer (Section G): TELEFLEX MEDICAL SDN. BHD.; lot no : pt2577 jalen perusahaan; 4 kamunting industrial estate; perak, west malaysia 34600 ; MY 34600
• Manufacturer Contact: katharine tarpley ; 3015 carrington mill blvd; morrisville, NC 27560
• MDR Report Key: 16796009
• Report Number: 8040412-2023-00187
• Device Sequence Number: 12359118
• Product Code: EZL
• UDI-Device Identifier: 04026704335046
• UDI-Public: 04026704335046
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/06/2023

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
• Operator of Device: Health Professional
• Device Model Number: IPN050272
• Device Catalogue Number: 171305-000180
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/06/2023
• Supplement Date Received by Manufacturer: 05/26/2023
• Initial Report FDA Received Date: 04/24/2023
• Supplement Report FDA Received Date: 05/30/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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