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Catalog Number SGC0701 |
Device Problem
Leak/Splash (1354)
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Patient Problems
Air Embolism (1697); Non specific EKG/ECG Changes (1817)
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Event Date 10/16/2023 |
Event Type
Injury
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Manufacturer Narrative
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The device has been received.However, investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.The additional mitraclip device referenced in b5 is being filed under a separate medwatch report.
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Event Description
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It was reported this was a mitraclip procedure to treat functional mitral regurgitation (mr) with a grade of 4.A steerable guide catheter (sgc) (30622r1061) was inserted and placed in the left atrium.However, when inserting an xtw clip (30710a1089) into the sgc, air in the fluid column was observed.The clip was removed and re-inserted, but the air remained.Therefore, the clip was removed and the sgc was replaced.The same clip was re-inserted into a new sgc, however, air remained.Therefore, the clip was removed and replaced.The procedure was continued with the new sgc and a new clip.The new clip was successfully implanted, reducing mr to a grade of 1.It was noted air entered the anatomy and was removed naturally from the anatomy.A sign of st-elevation of an electrocardiogram (ekg) was observed, which returned to normal.For treatment, oxygen was administered to the patient.There was no clinically significant delay in the procedure.No additional information was provided.
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Manufacturer Narrative
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All available information was investigated, and the reported loss of fluid column was not confirmed via returned device analysis.A review of the lot history record revealed no manufacturing nonconformities issued to the reported lot that would have contributed to this event.Additionally, a review of the complaint history did not indicate a lot-specific quality issue.Based on available information and the returned device analysis, the cause of the reported loss of fluid column was unable to be determined.The reported air embolism and ekg/ecg changes are cascading events of the reported loss of fluid column.The reported patient effects of ekg/ecg changes (cardiac arrhythmias) and embolism, as listed in the mitraclip system instructions for use, are known possible complications associated with mitraclip procedures.The reported unexpected medical intervention was a result of case-specific circumstances.There is no indication of a product quality issue with respect to manufacture, design, or labeling.
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Search Alerts/Recalls
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