MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION MUSTANG?; STENTS, DRAINS AND DILATORS FOR THE BILIARY DUCTS

Model Number	H74939171040410
Medical Device Problem Codes	Material Rupture (1546); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/28/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
D2b: pro code (product code): fge, lit.G4: premarket/510(k) #: k103751, k110122.
Event or Problem Description
It was reported that a balloon rupture occurred.The 70% stenosed target lesion was located in the moderately tortuous and moderately calcified superficial femoral artery.A 4.0 x 40, 135 cm mustang balloon catheter was advanced for dilation.During the procedure, the balloon ruptured upon second inflation at 18 atmospheres for 1 minute.The device was removed without any problem, and the procedure was completed with a different device.There were no patient complications as a result of this event.
Event or Problem Description
It was reported that a balloon rupture occurred.The 70% stenosed target lesion was located in the moderately tortuous and moderately calcified superficial femoral artery.A 4.0 x 40, 135cm mustang balloon catheter was advanced for dilation.During the procedure, the balloon ruptured upon second inflation at 18 atmospheres for 1 minute.The device was removed without any problem, and the procedure was completed with a different device.There were no patient complications as a result of this event.
Additional Manufacturer Narrative
D2b - pro code (product code): fge, lit.G4 - premarket / 510(k) #: k103751, k110122.Device evaluated by mfr: the mustang device was returned to our post market quality assurance laboratory.A visual examination identified that the balloon was not folded which indicates that the balloon was subjected to positive pressure.A full balloon circumferential tear was identified located approximately 5mm proximal of the distal balloon markerband.A visual and tactile examination identified shaft stretching and shaft damage.Both markerbands were present on the shaft of the device.The proximal markerband seemed to have part of the shaft that was stretched partly covering it.A visual examination observed no damage to the tip of the device.This concludes the product analysis.

• Brand Name: MUSTANG?
• Common Device Name: STENTS, DRAINS AND DILATORS FOR THE BILIARY DUCTS
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; pmt 741 persiaran cassia selat; bandarcassia, pulau pinan 14110 ; MY 14110
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 22182966
• Report Number: 2124215-2025-38297
• Device Sequence Number: 8356597
• Product Code: FGE
• UDI-Device Identifier: 08714729793557
• UDI-Public: (01)08714729793557(17)280212(10)35838630
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: K103751
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 08/18/2025

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: H74939171040410
• Device Catalogue Number: H74939171040410
• Device Lot Number: 0035838630
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/28/2025
• Supplement Date Received by Manufacturer: 07/31/2025
• Initial Report FDA Received Date: 06/11/2025
• Supplement Report FDA Received Date: 08/18/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/12/2025
• 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: 75 YR
• Patient Sex: Male