Catalog Number CDS0702-XTW |
Device Problem
Incomplete Coaptation (2507)
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Patient Problem
Mitral Valve Insufficiency/ Regurgitation (4451)
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Event Date 01/17/2024 |
Event Type
Injury
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Manufacturer Narrative
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The device was not returned for 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, the cause of the reported slda was unable to be determined.The reported recurrent mr was a cascading event of the reported slda.The reported patient effect of mitral regurgitation, as listed in the mitraclip system instructions for use, is a known possible complication associated with mitraclip procedures.The reported unexpected medical intervention and hospitalization were results of case-specific circumstances.There is no indication of a product quality issue with respect to manufacture, design, or labeling.
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Event Description
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It was reported that on (b)(6) 2024, a mitraclip procedure was performed to mixed degenerative mitral regurgitation (mr) with a grade of 3-4.One clip was implanted, reducing mr to a grade of 1.On 17jan2024, echocardiography showed the implanted clip had detached from the posterior leaflet and remained attached to the anterior leaflet (single leaflet device attachment/slda), causing mr to increase to 3.On (b)(6) 2024, a second mitraclip procedure was performed in an attempt to stabilize the slda.However, the mitraclip was unable to be implanted and mr remained at a grade of 3.
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Search Alerts/Recalls
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