Model Number 620RG29 |
Device Problems
Patient-Device Incompatibility (2682); Insufficient Information (3190)
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Patient Problem
No Information (3190)
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Event Type
Injury
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Manufacturer Narrative
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Without the return of the product, no definitive conclusion can be made regarding the clinical observation.If information is provided in the future, a supplemental report will be issued.
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Event Description
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Medtronic received information that during the implant of this annuloplasty ring, the ring was explanted and replaced.The reason for replacement was not reported.No adverse patient effects were reported.
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Manufacturer Narrative
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Medtronic received information that the ring was explanted because the repair was not to the satisfaction of the surgeon.If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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