MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION MUSTANG; CATHETER, BILIARY, DIAGNOSTIC

Model Number	24674
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/18/2022
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred the occluded target lesion was located in iliac femoral vein.A 10.0 x 80, 135cm mustang balloon catheter was advanced for dilatation.However, before the pressure reaching the standard, the balloon ruptured.The device was removed from the body immediately.The procedure was completed with another of same device.There were no patient complications reported and the patient was in stable condition.
Event or Problem Description
It was reported that balloon rupture occurred.The occluded target lesion was located in iliac femoral vein.A 10.0 x 80, 135cm mustang balloon catheter was advanced for dilatation.However, before the pressure reaching the standard, the balloon ruptured.The device was removed from the body immediately.The procedure was completed with another of same device.There were no patient complications reported and the patient was in stable condition.It was further reported that the lesion was moderately stenosed, non-calcified, non-tortuous and with no significant bend.The balloon ruptured during the initial inflation at 5-6 atmospheres.
Additional Manufacturer Narrative
Device evaluated by mfr.: a mustang device was received for analysis.A visual examination identified that the balloon was not folded which indicates that the balloon was subjected to positive pressure.A longitudinal tear was identified in the balloon material.The tear measured 75mm in length and extended from a position 3mm distal of the proximal markerband to 6mm distal of the distal markerband.An examination of the balloon material and markerbands identified no issues which could potentially have contributed to this complaint.A visual examination observed no damage to the tip of the device.A visual and tactile examination found no kinks or damage to the shaft of the device.Both markerbands were undamaged and present on the shaft of the device.This concludes the product analysis.
Event or Problem Description
It was reported that balloon rupture occurred the occluded target lesion was located in iliac femoral vein.A 10.0 x 80, 135cm mustang balloon catheter was advanced for dilatation.However, before the pressure reaching the standard, the balloon ruptured.The device was removed from the body immediately.The procedure was completed with another of same device.There were no patient complications reported and the patient was in stable condition.It was further reported that the lesion was moderately stenosed, non-calcified, non-tortuous and with no significant bend.The balloon ruptured during the initial inflation at 5-6 atmospheres.

• Brand Name: MUSTANG
• Common Device Name: CATHETER, BILIARY, DIAGNOSTIC
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; pmt 741 persiaran cassia selat; bandarcassia, pulau pinan 14110 ; MY 14110
• Manufacturer Contact: jay johnson ; 4100 hamline ave n; arden hills, MN 55112 ; 6515810888
• MDR Report Key: 15668593
• Report Number: 2124215-2022-43243
• Device Sequence Number: 20444052
• Product Code: FGE
• UDI-Device Identifier: 08714729795254
• UDI-Public: 08714729795254
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K141521
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/02/2023

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 Expiration Date: 09/16/2024
• Device Model Number: 24674
• Device Catalogue Number: 24674
• Device Lot Number: 0028038123
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 10/20/2022
• Supplement Date Received by Manufacturer: 10/26/2022; 02/28/2023
• Initial Report FDA Received Date: 10/25/2022
• Supplement Report FDA Received Date: 11/01/2022; 03/02/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/17/2021
• 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 Age: 56 YR
• Patient Sex: Male
• Patient Weight: 75 KG