The complainant was unable to provide the device lot number; therefore, the lot expiration and device manufacture dates are unknown.(b)(4).The device has not been received for analysis.Upon receipt and completion of the device analysis, if there is any further relevant information from that review, a supplemental medwatch will be filed.
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It was reported to boston scientific corporation, through a post market clinical follow up (pmcf) of retrospective data collection, that a lithovue flexscope was used during a cystourethroscopy with left ureteral stent placement, left ureteroscopy with laser lithotripsy procedure performed on (b)(6) 2021.During the procedure as the access sheath was pulled back a tear was noted through the patient's ureter at around the mid to proximal ureter.
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