Home/Recalls/CANADA-58819
Health CanadaGeneral Alert

XARELTO (rivaroxaban) - Increase in all-cause mortality, thromboembolic and bleeding events in patients after transcatheter aortic valve replacement

Published: December 20, 2018Recall ID: 58819Category: generalCountry: Canada
Canada
Safety AlertHealth CanadaCanadaCanada

XARELTO (rivaroxaban) - Increase in all-cause mortality, thromboembolic and bleeding events in patients after transcatheter aortic valve replacement

Recalling Firm: Marketed health products

Reason for Recall / Hazard

Product safety

Product Description & Identification

XARELTO (rivaroxaban) - Increase in all-cause mortality, thromboembolic and bleeding events in patients after transcatheter aortic valve replacement

Additional Source Details

FieldValue
N I D58819
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/xarelto-rivaroxaban-increase-all-cause-mortality-thromboembolic-and-bleeding-events
IssueProduct safety
Title XARELTO (rivaroxaban) - Increase in all-cause mortality, thromboembolic and bleeding events in patients after transcatheter aortic valve replacement
Archived0
CategoryDrugs
Last updated2018-12-20
OrganizationMarketed health products

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Overview

  • Recalling FirmMarketed health products
Recall Hazard Severity
Caution (Class III)
Official Agency Alert

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🚨 SAFETY ALERT: Marketed health products - XARELTO (rivaroxaban) - Increase in all-cause mortality, thromboembolic and bleeding events in patients after transcatheter aortic valve replacement

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