Model Number 0010-2400 |
Device Problems
Break (1069); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/08/2024 |
Event Type
malfunction
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Manufacturer Narrative
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This report is for the same event as manufacturer report: 2124215-2024-13814.
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Event Description
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It was reported that, during the photoselective vaporization of the prostate procedure, two fibers broke on the inside of the protection device after several minutes of use.The procedure was then switched to bipolar resection.Boston scientific has been unable to obtain additional information regarding the patient outcome to date, despite good faith efforts.This report is for the first fiber.
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Manufacturer Narrative
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This report is for the same event as manufacturer report: 2124215-2024-13814.Upon receipt at our quality assurance laboratory, the fiber was thoroughly analyzed.Visual examination identified the glass cap and metal cap were detached and were not returned with the fiber.The fiber was functionally tested with the hene (helium-neon) laser fixture.The testing conducted showed there were no additional breakages along the length of the fiber.The connector cone, segments, and tabs appear in good condition and are secured.The fiber passed the connector segment verification test.The control knob is attached and aligned with the fiber and can rotate the fiber.It is probable that the glass cap and metal cap detachment occurred due to inadvertent heavy tissue contact and a decrease in saline flow.The interaction between the user and device caused or contributed to the observed fiber tip damage and reported event.According to the instructions for use, increased irrigation flow by means of a saline pressure bag (set to 250 mmhg - 300 mmhg) will further increase liquid cooling effect and may reduce fiber tip damage.
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Event Description
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It was reported that, during the photoselective vaporization of the prostate procedure, two fibers broke on the inside of the protection device after several minutes of use.The procedure was then switched to bipolar resection.Boston scientific has been unable to obtain additional information regarding the patient outcome to date, despite good faith efforts.This report is for the first fiber.
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Search Alerts/Recalls
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