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Model Number M00565040 |
Device Problems
Break (1069); Positioning Failure (1158); Material Deformation (2976)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 05/22/2023 |
Event Type
malfunction
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Manufacturer Narrative
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Block h6: impact code f1001 is being used to capture the reportable event of cancelled or rescheduled procedure.
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Event Description
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Note: this report pertains to one of the four devices used on the same patient.Refer to manufacturer report# 3005099803-2023-03080, 3005099803-2023-03082, and 3005099803-2023-03083 for the associated device in formation.It was reported to boston scientific corporation on (b)(6) 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 mfr.Report # 3005099803-2023-03080) did not deploy, the handle broke, and the stainless-steel shaft was kinked.A second wallflex colonic stent (the subject of this report) 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.
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Manufacturer Narrative
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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, and the outer blue sheath was detached from the control hub handle.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 and handle break; however, the reported event of stainless-steel shaft kinking was not confirmed.The investigation concluded that the reported events and the additional finding of sheath kinking were most likely due to procedural factors.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.
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Event Description
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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 in formation.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 mfr.Report # 3005099803-2023-03080) did not deploy, the handle broke, and the stainless-steel shaft was kinked.A second wallflex colonic stent (the subject of this report) 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.
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Search Alerts/Recalls
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