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Health CanadaGeneral Alert

Casirivimab and Imdevimab – High Risk of Treatment Failure Due to Circulation of...

Published: January 7, 2022Recall ID: 63799Category: generalCountry: Canada

Reason for Recall / Hazard

New safety information - COVID

Product Description & Identification

Casirivimab and Imdevimab – High Risk of Treatment Failure Due to Circulation of SARS-CoV-2 Omicron Variant

Affected Products

Casirivimab and Imdevimab

Additional Source Details

FieldValue
N I D63799
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/casirivimab-and-imdevimab-high-risk-treatment-failure-due-circulation-sars-cov-2
IssueNew safety information - COVID
TitleCasirivimab and Imdevimab – High Risk of Treatment Failure Due to Circulation of SARS-CoV-2 Omicron Variant
ProductCasirivimab and Imdevimab
Archived0
CategoryBiologic or vaccine
Last updated2022-01-07
OrganizationMarketed health products

Overview

  • Recalling FirmMarketed health products
Official Agency Alert