MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION VENOUS WALLSTENT; STENT, ILIAC VEIN

Model Number	H74912044208070
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/30/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the balloon was stuck on the distal end of the stent, necessitating additional intervention.The target lesion was located in the left common iliac vein, which was mildly tortuous, compressed, and calcified.A 20x80x75cm venous wallstent was placed by the physician to extend a previously placed stent in the left common iliac vein.The physician post-dilated the lesion using an 18x4x75 xxl balloon catheter and attempted to reposition the stent during balloon inflation.However, the balloon became stuck at the distal end of the wallstent and would not release.When applied more force, the entire balloon detached from the catheter shaft.Efforts to snare and remove the balloon were unsuccessful.The balloon lodged between the vessel wall and the first placed wallstent in the left common iliac vein.After unsuccessful removal attempts, the physician decided it would be best to leave the balloon captured between the stent and the vessel wall, as it was immovable, and the patient was asymptomatic following the procedure.The procedure was completed and there were no complications were reported.

• Brand Name: VENOUS WALLSTENT
• Common Device Name: STENT, ILIAC VEIN
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC IRELAND LIMITED; ballybrit business park; galway ; EI
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 19361307
• Report Number: 2124215-2024-30921
• Device Sequence Number: 3798439
• Product Code: QAN
• UDI-Device Identifier: 08714729979647
• UDI-Public: 08714729979647
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: P980033/S050
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 05/21/2024

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 Model Number: H74912044208070
• Device Catalogue Number: H74912044208070
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/30/2024
• Initial Report FDA Received Date: 05/21/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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