Note: this report pertains to one of five sensation short throws used in the same procedure.It was reported to boston scientific corporation that a sensation medium oval flexible snare was used during an endoscopic mucosal resection procedure performed on (b)(6) 2023.During the procedure, when the handle was tightened all the way, the polyp could not be removed.It was noted that the outer sheath at the front end of the device was found to be shorter when fully withdrawn when compared to the device used to complete the procedure.The procedure was completed with a similar sensation short throw.There were no patient complications reported as a result of this event.
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Note: this report pertains to one of five sensation short throws used in the same procedure.It was reported to boston scientific corporation that a sensation medium oval flexible snare was used during an endoscopic mucosal resection procedure performed on (b)(6) 2023.During the procedure, when the handle was tightened all the way, the polyp could not be removed.It was noted that the outer sheath at the front end of the device was found to be shorter when fully withdrawn when compared to the device used to complete the procedure.The procedure was completed with a similar sensation short throw.There were no patient complications reported as a result of this event.
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Block e1: (initial reporter facility) (b)(6).Block e1: (initial reporter city) (b)(6).Block h6: imdrf device code a050702 captures the reportable event of loop unable to cut.Block h10 investigation results: one sensation snare was received for analysis.Upon visual inspection, there were no damages found.During functional evaluation, the device showed that it could extend and retract well when connected to the 10-inch loop fixture.During the dimensional test, the device was within specification.No other issues were observed.The reported event of "loop failure to cut" could not be confirmed, as it was not possible to evaluate the device's function during the specific procedure.It is possible that procedural factors, such as physician technique or handling of the device during initial use or setup, may have contributed to the device's condition.The product record review revealed that this was not a new failure type, and the risk had been anticipated.There was no evidence of a manufacturing, design, or user problem that could have caused the complaint.Device analysis showed no issues during visual, functional, and dimensional testing.Based on the available information and device analysis, the most probable root cause for the reported complaint is "no problem detected." a review of the device history record (dhr) confirmed that the device met all material, assembly, and performance specifications at the time of release for distribution.
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Note: this report pertains to one of five sensation short throws used in the same procedure.It was reported to boston scientific corporation that a sensation medium oval flexible snare was used during an endoscopic mucosal resection procedure performed on (b)(6) 2023.During the procedure, when the handle was tightened all the way, the polyp could not be removed.It was noted that the outer sheath at the front end of the device was found to be shorter when fully withdrawn when compared to the device used to complete the procedure.The procedure was completed with a similar sensation short throw.There were no patient complications reported as a result of this event.
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