Date of death: date of death estimated.Date of event: date of event estimated.The udi is unknown because the part number and lot number were not provided.Date of implant: implant date estimated.The device was not returned for evaluation.A review of the lot history record of the reported lot could not be conducted because the part and lot number were not provided.The reported patient effect of death is listed in the xience v and xience nano everolimus eluting coronary stent systems instructions for use as a known patient effect of coronary procedures.A conclusive cause for the reported death and the relationship to the product, if any, cannot be determined.There is no indication of a product quality issue with respect to manufacture, design or labeling.The adverse patient effects referenced is being filed under a separate medwatch report number.Literature title : everolimus-eluting stents or bypass surgery for left main coronary artery disease.
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It was reported through a research article identifying that xience stents may be related to the following: death, myocardial infarction, stroke, ischemia, thrombosis, bleeding, revascularization and rehospitalization.This article summarizes clinical outcomes of 1905 patients that were treated with xience stents.Specific patient information is documented as unknown.Details are listed in the attached article, titled "everolimus-eluting stents or bypass surgery for left main coronary artery disease.".
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