MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION ADVANIX? PANCREATIC STENT; CATHETER, BILIARY, DIAGNOSTIC

Model Number	M00536890
Medical Device Problem Code	Material Deformation (2976)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/04/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
H6: imdrf device code a0406 captures the reportable event of stent kinked.
Event or Problem Description
It was reported to boston scientific corporation that an advanix pancreatic stent was to be implanted during an endoscopic retrograde pancreatic drainage (erpd) procedure performed on (b)(6) 2025.During procedure, the distal part of the stent was bent.The procedure was completed using another of the same device.There were no patient complications reported as a result of the procedure.
Event or Problem Description
It was reported to boston scientific corporation that an advanix pancreatic stent was to be implanted during an endoscopic retrograde pancreatic drainage (erpd) procedure performed on (b)(6) 2025.During procedure, the distal part of the stent was bent.The procedure was completed using another of the same device.There were no patient complications reported as a result of the procedure.
Additional Manufacturer Narrative
Block e1: initial reporter phone number has been corrected.Block h6: imdrf device code a0406 captures the reportable event of stent kinked.

• Brand Name: ADVANIX? PANCREATIC STENT
• 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; 780 brookside drive; spencer IN 47460
• Manufacturer Contact: christina lam ; 300 boston scientific way; marlborough, MA 01752 ; 9145716918
• MDR Report Key: 23927681
• Report Number: 3005099803-2025-06941
• Device Sequence Number: 18395441
• Product Code: FGE
• UDI-Device Identifier: 08714729856481
• UDI-Public: (01)08714729856481(17)260918(10)36103567
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: K133700
• 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): 03/31/2026

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: 09/18/2026
• Device Model Number: M00536890
• Device Catalogue Number: M00536890
• Device Lot Number: 0036103567
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/04/2025
• Supplement Date Received by Manufacturer: 03/10/2026
• Initial Report FDA Received Date: 12/30/2025
• Supplement Report FDA Received Date: 03/31/2026
• Date Device Manufactured: 03/19/2025
• 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 Sex: Unknown