MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION 2CM PERIPHERAL CUTTING BALLOON; CATHETER, PERCUTANEOUS, CUTTING/SCORING

Model Number	24634
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/22/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon burst occurred.The occluded target lesion was located in the mildly tortuous fistula in the upper extremity.A 6.00mm/2.0cm/135cm peripheral cutting balloon catheter was advanced across the narrow arterial anastomosis.During several dilation, the balloon would not inflate above 5 atmospheres and would not hold that pressure.It was determined that the balloon must have burst.The balloon was pulled out of the sheath and used a plain old balloon angioplasty to complete the procedure.There was no device fragments left inside the patient.No patient complications were reported.
Additional Manufacturer Narrative
Device evaluation by manufacturer: upon receipt at our post market quality assurance laboratory, a visual examination identified that the balloon was not folded which indicates that the device was subjected to positive pressure.The rated burst pressure for this device is 10 atmospheres as per pcb2cm specification.The returned device was attached to an encore inflation unit.Positive pressure was applied when di water was observed to be leaking from a balloon pinhole located approximately 12mm distal of the proximal markerband.A visual examination observed no damage to the tip or blades.All blades were present and fully bonded to the balloon surface.A visual and tactile examination identified no kinks or damage to the shaft of the device.This concludes the product analysis.
Event or Problem Description
It was reported that balloon burst occurred.The occluded target lesion was located in the mildly tortuous fistula in the upper extremity.A 6.00mm/2.0cm/135cm peripheral cutting balloon catheter was advanced across the narrow arterial anastomosis.During several dilation, the balloon would not inflate above 5 atmospheres and would not hold that pressure.It was determined that the balloon must have burst.The balloon was pulled out of the sheath and used a plain old balloon angioplasty to complete the procedure.There was no device fragments left inside the patient.No patient complications were reported.It was further reported that the balloon burst was confirmed, as the contrast was noted to be coming out of the balloon.The balloon was inflated twice up to 4 atmospheres when it ruptured.The blades were unable to fold completely during removal, causing the sheath to be sliced on the way out.

• Brand Name: 2CM PERIPHERAL CUTTING BALLOON
• Common Device Name: CATHETER, PERCUTANEOUS, CUTTING/SCORING
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; ballybrit business park; galway ; EI
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 21393828
• Report Number: 2124215-2025-09125
• Device Sequence Number: 8526248
• Product Code: PNO
• UDI-Device Identifier: 08714729813729
• UDI-Public: 08714729813729
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K151253
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 03/11/2025

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 Expiration Date: 05/08/2025
• Device Model Number: 24634
• Device Catalogue Number: 24634
• Device Lot Number: 0031580306
• 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: 02/03/2025
• Supplement Date Received by Manufacturer: 02/21/2025
• Initial Report FDA Received Date: 02/18/2025
• Supplement Report FDA Received Date: 03/11/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/09/2023
• 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: 49 YR
• Patient Sex: Male
• Patient Race: White