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

Model Number	24674
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Codes	No Consequences Or Impact To Patient (2199); No Known Impact Or Consequence To Patient (2692)
Date of Event	12/30/2019
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred.The target lesion was located in the external iliac artery.A 8.0x80, 135cm mustang balloon catheter was advanced for dilatation.However, during inflation, the balloon ruptured.No patient complications were reported.
Additional Manufacturer Narrative
Device evaluated b mfr.: mustang 8.0 x 80, 135cm was returned for analysis.Blood was identified in the balloon which is indicative of a leak.The returned device was loaded onto a mandrel and attached to an encore inflation unit.Positive pressure was applied, and a pinhole leak was identified 8 mm proximal of the distal markerband.No other issues were noted.A visual and microscopic examination of the balloon material identified no issues that could have contributed to the complaint incident.A visual and microscopic examination of the markerbands identified no issues which may potentially have contributed to the complaint incident.A visual and tactile examination identified no kinks or damage to the shaft which may have potentially contributed to the complaint incident.A visual and tactile examination identified no damage to the tip which may have potentially contributed to the complaint incident.No other issues were identified during the product analysis.
Event or Problem Description
It was reported that balloon rupture occurred.The target lesion was located in the external iliac artery.An 8.0x80, 135cm mustang balloon catheter was advanced for dilatation.However, during inflation, the balloon ruptured.No patient complications were reported.It was further reported that the target lesion was 80% stenosed, located in the mildly tortuous and severely calcified iliac artery.The patient's condition following procedure was good.
Event or Problem Description
It was reported that balloon rupture occurred.The target lesion was located in the external iliac artery.An 8.0x80, 135cm mustang balloon catheter was advanced for dilatation.However, during inflation, the balloon ruptured.No patient complications were reported.It was further reported that the target lesion was 80% stenosed, located in the mildly tortuous and severely calcified iliac artery.The patient's condition following procedure was good.
Additional Manufacturer Narrative
(b5) describe event or problem updated.(f10) patient code updated.

• Brand Name: MUSTANG
• Common Device Name: CATHETER, BILIARY, DIAGNOSTIC
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• MDR Report Key: 9708474
• Report Number: 2134265-2020-01522
• Device Sequence Number: 3675764
• Product Code: FGE
• UDI-Device Identifier: 08714729794301
• UDI-Public: 08714729794301
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: K141521
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/31/2020

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: 11/25/2021
• Device Model Number: 24674
• Device Catalogue Number: 24674
• Device Lot Number: 0022986569
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/26/2020
• Initial Date Received by Manufacturer: 01/29/2020
• Supplement Date Received by Manufacturer: 02/13/2020; 03/19/2020
• Initial Report FDA Received Date: 02/13/2020
• Supplement Report FDA Received Date: 03/09/2020; 03/31/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 83 YR