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Health CanadaGeneral Alert

Sotrovimab for Injection - Risk of Treatment Failure due to Circulation of SARS...

Published: April 14, 2022Recall ID: 64084Category: generalCountry: Canada

Reason for Recall / Hazard

New safety information - COVID

Product Description & Identification

Sotrovimab for Injection - Risk of Treatment Failure due to Circulation of SARS-CoV-2 Omicron BA.2 Subvariant

Affected Products

Sotrovimab, 500 mg IV

Additional Source Details

FieldValue
N I D64084
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/sotrovimab-injection-risk-treatment-failure-due-circulation-sars-cov-2-omicron-ba2
IssueNew safety information - COVID
TitleSotrovimab for Injection - Risk of Treatment Failure due to Circulation of SARS-CoV-2 Omicron BA.2 Subvariant
ProductSotrovimab, 500 mg IV
Archived0
CategoryBiologic or vaccine
Last updated2022-04-14
OrganizationMarketed health products

Overview

  • Recalling FirmMarketed health products
Official Agency Alert