MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION QUANTUM MAVERICK; CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS

Model Number	H7493808015250
Medical Device Problem Codes	Nonstandard Device (1420); Material Rupture (1546)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/21/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred.The 80% stenosed target lesion was located in the moderately tortuous and severely calcified left anterior descending artery.A 2.5mm x 15mm quantum maverick balloon catheter was advanced for dilation.However, during first inflation at 12 atmospheres, the balloon ruptured.The procedure was completed with another of same device.There were no patient complications.Patient was stable.
Additional Manufacturer Narrative
E.1.: initial reporter facility name, address, and phone number: (b)(6).
Event or Problem Description
It was reported that balloon rupture occurred.The 80% stenosed target lesion was located in the moderately tortuous and severely calcified left anterior descending artery.A 2.5mm x 15mm quantum maverick balloon catheter was advanced for dilation.However, during first inflation at 12 atmospheres, the balloon ruptured.The procedure was completed with another of same device.There were no patient complications.Patient was stable.
Additional Manufacturer Narrative
E1: initial reporter facility name: (b)(6) hospital.E1: initial reporter address 1: (b)(6).E1: initial reporter phone: (b)(6).
Additional Manufacturer Narrative
E1: initial reporter facility name: (b)(6).E1: initial reporter address 1: no.(b)(6).E1: initial reporter phone: (b)(6).Device evaluated by mfr: fg quantum maverick, mr 2.5mm x 15mm was returned for analysis.A visual and tactile examination identified multiple kinks along the length of the hypotube shaft.A visual inspection of the outer and inner lumen and tactile examination of the entire extrusion found no issues.Microscopic examination of the balloon material identified a pinhole leak approximately 3mm proximal to the distal markerband.Bumper tip showed no signs of distal tip damage.The device was attached to an encore inflation device.An attempt was then made to inflate the balloon; however, it was observed that a leak was occurring.An image was provided which shows the balloon of the device however there is no obvious visible damage.This returned media cannot confirm the reported allegation.
Event or Problem Description
It was reported that balloon rupture occurred.The 80% stenosed target lesion was located in the moderately tortuous and severely calcified left anterior descending artery.A 2.5mm x 15mm quantum maverick balloon catheter was advanced for dilation.However, during first inflation at 12 atmospheres, the balloon ruptured.The procedure was completed with another of same device.There were no patient complications.Patient was stable.

• Brand Name: QUANTUM MAVERICK
• Common Device Name: CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS
• 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: mark mischke ; 4100 hamline ave n; arden hills, MN 55112 ; 7634941632
• MDR Report Key: 23065939
• Report Number: 2124215-2025-64838
• Device Sequence Number: 10044847
• Product Code: LOX
• UDI-Device Identifier: 08714729392767
• UDI-Public: (01)08714729392767(17)280210(10)35816085
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: P860019
• 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): 11/26/2025

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: H7493808015250
• Device Catalogue Number: H7493808015250
• Device Lot Number: 0035816085
• 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: 08/28/2025
• Supplement Date Received by Manufacturer: 09/12/2025; 11/06/2025
• Initial Report FDA Received Date: 09/16/2025
• Supplement Report FDA Received Date: 09/29/2025; 11/26/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/10/2025
• 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: 70 YR
• Patient Sex: Male
• Patient Weight: 60 KG