Model Number D138502 |
Device Problems
Break (1069); Material Perforation (2205)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 08/25/2021 |
Event Type
malfunction
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Manufacturer Narrative
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If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.If additional information is received regarding this event, a supplemental 3500a report will be submitted to the fda.Manufacturer's reference number: (b)(4).
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Event Description
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It was reported that an unknown patient underwent an unknown ablation procedure with (2) carto vizigo¿ 8.5f bi-directional guiding sheath ¿ medium.A piece of grey plastic was removed.Physician tried to do the transeptal puncture and unfortunately removed some pieces of grey plastic, probably from the dilator.The procedure was delayed 5 minutes due to the reported event.Perforation of dilator is mdr-reportable.This report is for the 1st of 2 reportable carto vizigo¿ 8.5f bi-directional guiding sheath ¿ medium.The other complaint device was reported under manufacturer report number 2029046-2021-01597.
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Manufacturer Narrative
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On (b)(6)-2021, the bwi product analysis lab received the device for evaluation.The analysis has begun but is not completed at this time.When the investigational analysis has been completed, a supplemental 3500a report will be submitted.If additional information is received regarding this event, a supplemental 3500a report will be submitted to the fda.Manufacturer's reference number: (b)(4).
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Manufacturer Narrative
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On(b)(6)2021, bwi received additional information regarding the event.It was confirmed that the pieces were related to the dilator.No perforation or foreign material were identified.Subsequently, the product investigation was completed.Device evaluation details: the product was returned to biosense webster for evaluation.Bwi conducted a visual inspection of the returned product.Visual analysis of the returned sample revealed that no damage or anomalies were observed on the vizigo sheath.A device history record was performed for the finished device 00001456 number, and no internal actions related to the reported complaint condition were identified.No issues were verified during the analysis.Although no product defect was identified, there may have been other circumstances or issues that occurred during the use of the device that could not be replicated during the analysis.If additional information is received regarding this event, a supplemental 3500a report will be submitted to the fda.Manufacturer's reference number: (b)(4).
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Manufacturer Narrative
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Per internal review on (b)(6)2021, it was determined that the previously reported medical device problem code (section h6) for "material perforation" (a0410) is not the most fitting code.It has been determined that the "break" (a0401) code is the most fitting code for this event.If additional information is received regarding this event, a supplemental 3500a report will be submitted to the fda.Manufacturer's reference number: (b)(4).
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Search Alerts/Recalls
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