MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION INNOVA VASCULAR; STENT, SUPERFICIAL FEMORAL ARTERY

Model Number 26924

Device Problem Positioning Problem (3009)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 05/04/2023

Event Type  Injury  

Event Description

It was reported that the stent jumped.A 6mm x 40mm x 75cm innova self-expanding stent was selected for use in a left upper extremity fistulagram with angioplasty and stenting.There was tight stenosis in the distal portion of the left upper extremity fistula, which was pre-dilated with a 6mm x 40mm gladiator balloon.The physician was in the process of deploying the innova stent, but the stent released and migrated to the auxiliary vein before finishing deployment.A 7mm x 40mm gladiator balloon was used to pull the stent back down towards the lesion.It stopped proximal to the lesion.A 7mm x 40mm innova stent was then used to both cover the stenotic lesion and secure the previously deployed 6mm x 40mm innova stent in place just above the lesion.No patient complications were reported.

• Brand Name: INNOVA VASCULAR
• Type of Device: STENT, SUPERFICIAL FEMORAL ARTERY
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• Manufacturer Contact: jeff wallner ; 4100 hamline ave n; arden hills, MN 55112 ; 6515811560
• MDR Report Key: 17101392
• MDR Text Key: 316931604
• Report Number: 2124215-2023-29308
• Device Sequence Number: 1
• Product Code: NIP
• UDI-Device Identifier: 08714729873631
• UDI-Public: 08714729873631
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P140028
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 06/09/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/09/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 26924
• Device Catalogue Number: 26924
• Device Lot Number: 0028160399
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 05/18/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/07/2021
• Is the Device Single Use?: Yes
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 61 YR
• Patient Sex: Female
• Patient Race: Black Or African American