Home/Recalls/CANADA-61726
Health CanadaGeneral Alert

FIBRISTAL (ulipristal acetate tablets, 5 mg) - Voluntary Withdrawal in Canada due to Risk of Drug-Induced Liver Injury

Published: September 30, 2020Recall ID: 61726Category: generalCountry: Canada
Canada
Safety AlertHealth CanadaCanadaCanada

FIBRISTAL (ulipristal acetate tablets, 5 mg) - Voluntary Withdrawal in Canada due to Risk of Drug-Induced Liver Injury

Recalling Firm: Marketed health products

Reason for Recall / Hazard

Product safety

Product Description & Identification

FIBRISTAL (ulipristal acetate tablets, 5 mg) - Voluntary Withdrawal in Canada due to Risk of Drug-Induced Liver Injury

Additional Source Details

FieldValue
N I D61726
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/fibristal-ulipristal-acetate-tablets-5-mg-voluntary-withdrawal-canada-due-risk-drug
IssueProduct safety
Title FIBRISTAL (ulipristal acetate tablets, 5 mg) - Voluntary Withdrawal in Canada due to Risk of Drug-Induced Liver Injury
Archived0
CategoryDrugs
Last updated2020-09-30
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 - FIBRISTAL (ulipristal acetate tablets, 5 mg) - Voluntary Withdrawal in Canada due to Risk of Drug-Induced Liver Injury

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https://therecallfile.com/recalls/fibristal-ulipristal-acetate-tablets-5-mg-voluntary-withdrawal-in-cana/CANADA-61726
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