MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION WALLFLEX COLONIC; STENT, COLONIC, METALIC, EXPANDABLE

Model Number M00565050

Device Problems Break (1069); Positioning Failure (1158); Material Deformation (2976)

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

Event Date 05/22/2023

Event Type  malfunction  

Event Description

Note: this report pertains to one of the four devices used on the same patient.Refer to manufacturer report#: 3005099803-2023-03081, 3005099803-2023-03082, and 3005099803-2023-03083 for the associated device information.It was reported to boston scientific corporation on may 24, 2023, that a wallflex enteral colonic stent was to be implanted in the sigmoid colon to treat a 6 cm malignant colonic obstruction during a colonoscopy with stent placement procedure performed on (b)(6)2023.The patient's anatomy was tight and was dilated prior to stent placement.During the procedure, the first wallflex colonic stent (the subject of this report) did not deploy, the handle broke, and the stainless-steel shaft was kinked.A second wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03081) was used, but similar issue was encountered.The stent did not deploy, the handle broke, and the stainless-steel shaft kinked.A third wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03082) was used, but the stent did not deploy, and the stainless-steel shaft was kinked.A fourth wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03083) was used, but still the stent did not deploy, and the stainless-steel shaft kinked.Consequently, the procedure was not completed, and no secondary procedure was scheduled.There were no reported patient complications as a result of this event.

Manufacturer Narrative

Block h6: impact code f1001 is being used to capture the reportable event of cancelled or rescheduled procedure.

Manufacturer Narrative

Block h6: impact code f1001 is being used to capture the reportable event of canceled or rescheduled procedure.Block h10: the wallflex enteral colonic stent and delivery system were received for analysis.Visual inspection of the returned device found that the stent was fully covered and undeployed.The outer clear sheath was kinked, while the outer blue sheath was detached from the handle and stretched in the hub section.The stainless-steel handle was also slightly bent.Functional inspection was not performed due to the outer sheath's detachment from the handle.No other damages were noted on the stent or delivery system.Product analysis confirmed the reported events of stent failure to deploy, handle break, and stainless-steel shaft kink.The investigation concluded that the reported events and the additional findings of sheath kinked, and sheath stretched were most likely due to procedural factors that were encountered.It may be that lesion characteristics, handling of the device, and the technique used by the physician (amount of force applied), limit the performance of the device and could have resulted in the damages noted on the device and the stent's inability to deploy during the procedure.Therefore, a review and analysis of all available information indicated the most probable cause is adverse event related to procedure.A product labeling review identified that the device was used per the instructions for use (ifu)/product label.

Event Description

Note: this report pertains to one of the four devices used on the same patient.Refer to manufacturer report# 3005099803-2023-03080, 3005099803-2023-03081, 3005099803-2023-03082, and 3005099803-2023-03083 for the associated device information.It was reported to boston scientific corporation on may 24, 2023, that a wallflex enteral colonic stent was to be implanted in the sigmoid colon to treat a 6 cm malignant colonic obstruction during a colonoscopy with stent placement procedure performed on (b)(6) 2023.The patient's anatomy was tight and was dilated prior to stent placement.During the procedure, the first wallflex colonic stent (the subject of this report) did not deploy, the handle broke, and the stainless-steel shaft was kinked.A second wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03081) was used, but similar issue was encountered.The stent did not deploy, the handle broke, and the stainless-steel shaft kinked.A third wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03082) was used, but the stent did not deploy, and the stainless-steel shaft was kinked.A fourth wallflex colonic stent (the subject of mfr.Report # 3005099803-2023-03083) was used, but still the stent did not deploy, and the stainless-steel shaft kinked.Consequently, the procedure was not completed, and no secondary procedure was scheduled.There were no reported patient complications as a result of this event.

• Brand Name: WALLFLEX COLONIC
• Type of Device: STENT, COLONIC, METALIC, EXPANDABLE
• 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: carole morley ; 300 boston scientific way; marlborough, MA 01752 ; 5086834015
• MDR Report Key: 17098577
• MDR Text Key: 317325682
• Report Number: 3005099803-2023-03080
• Device Sequence Number: 1
• Product Code: MQR
• UDI-Device Identifier: 08714729456520
• UDI-Public: 08714729456520
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K061877
• 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,Followup
• Report Date: 08/16/2023

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?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: M00565050
• Device Catalogue Number: 6505
• Device Lot Number: 0030390738
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 07/25/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 10/21/2022
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Sex: Female