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	03/15/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred.The 75% stenosed target lesion was located in the moderately tortuous and moderately calcified iliac artery.A 12.0 x 40, 135cm mustang balloon catheter was advanced for dilatation.However, during the first inflation at 8 atmospheres for 20 seconds, the balloon ruptured.The device was removed using normal method without issue and the procedure was completed with another of the same device.There were no complications reported and the patient was in good condition post procedure.
Additional Manufacturer Narrative
Corrected d4: lot number from 0030271538 to 0030391488.Corrected d4: expiration date from 10/03/2025 to 10/20/2025.Corrected h4: device manufacture date from 10/04/2022 to 10/21/2022.
Event or Problem Description
It was reported that balloon rupture occurred.The 75% stenosed target lesion was located in the moderately tortuous and moderately calcified iliac artery.A 12.0 x 40, 135cm mustang balloon catheter was advanced for dilatation.However, during the first inflation at 8 atmospheres for 20 seconds, the balloon ruptured.The device was removed using normal method without issue and the procedure was completed with another of the same device.There were no complications reported and the patient was in good condition post procedure.
Additional Manufacturer Narrative
Corrected d4: lot number from 0030271538 to 0030391488 corrected d4: expiration date from 10/03/2025 to 10/20/2025 corrected h4: device manufacture date from 10/04/2022 to 10/21/2022.Device evaluated by mfr: the device was returned for evaluation.A visual examination identified that the balloon was not folded which indicates that the balloon was subjected to positive pressure.The rated burst pressure for this device is 14 atmospheres as per mustang specification.The returned device was attached to an encore inflation unit.Positive pressure was applied when di water was observed to be leaking from the tip of the device.A visual examination of the markerbands identified no issues.A visual and tactile examination identified inner shaft damage.A visual and tactile examination identified no damage to the tip.No other issues were identified during the product analysis.
Event or Problem Description
It was reported that balloon rupture occurred.The 75% stenosed target lesion was located in the moderately tortuous and moderately calcified iliac artery.A 12.0 x 40, 135cm mustang balloon catheter was advanced for dilatation.However, during the first inflation at 8 atmospheres for 20 seconds, the balloon ruptured.The device was removed using normal method without issue and the procedure was completed with another of the same device.There were no complications reported and the patient was in good condition post procedure.

• Brand Name: MUSTANG
• Common Device Name: CATHETER, BILIARY, DIAGNOSTIC
• 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: 18948660
• Report Number: 2124215-2024-16988
• Device Sequence Number: 17905012
• Product Code: FGE
• UDI-Device Identifier: 08714729793953
• UDI-Public: 08714729793953
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• 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: Other,Foreign,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/03/2024

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: 10/20/2025
• Device Model Number: 24674
• Device Catalogue Number: 24674
• Device Lot Number: 0030391488
• 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: 03/15/2024
• Supplement Date Received by Manufacturer: 04/09/2024; 04/25/2024
• Initial Report FDA Received Date: 03/21/2024
• Supplement Report FDA Received Date: 04/22/2024; 05/03/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/21/2022
• 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
• Concomitant Medical Products and Therapy/Usage Dates: GUIDEWIRE: RADIFOCUS.; GUIDEWIRE: RADIFOCUS.; GUIDEWIRE: RADIFOCUS.; INTRODUCER SHEATH: 7 FR.; INTRODUCER SHEATH: 7 FR.; INTRODUCER SHEATH: 7 FR.
• Patient Sex: Unknown