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Catalog Number 150NSS35 |
Device Problem
Flaked (1246)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/21/2024 |
Event Type
malfunction
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Manufacturer Narrative
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The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.H11: section a through f - the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
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Event Description
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It was stated that in the same patient, in the same procedure, the guidewire was withdrawn after guiding the ureteroscope into the ureter, and the surface of the guidewire was wrinkled, making it impossible to guide the stent implantation any further.
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Search Alerts/Recalls
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