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Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Stenosis (2263)
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Event Date 09/07/2018 |
Event Type
Injury
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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During the index procedure the right anastomosis was treated with a medtronic standard pta.Approx.13 months post index procedure avf shunt stenosis was reported.The anastomosis was treated with a non-mdt pta.The patient was also treated with medication.The patient recovered.The investigator and safety assessed the event as not related to the index device, procedure or paclitaxel medication.
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Search Alerts/Recalls
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