Home/Recalls/CANADA-81592
Health CanadaType II

TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient tha...

Published: February 9, 2026Recall ID: 81592Category: generalCountry: Canada

Reason for Recall / Hazard

Product quality

Product Description & Identification

Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.Contact the recalling firm if you have any questions about the recall.Report any health product related side effects to Health Canada.Report any other health product safety complaints to Health Canada.

Affected Products

TARO-CANDESARTAN

Additional Source Details

FieldValue
N I D81592
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/taro-candesartan-affected-lots-were-manufactured-using-active-ingredient-was-out
IssueProduct quality
TitleTARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
ProductTARO-CANDESARTAN
Archived0
CategoryDrugs
Last updated2026-02-09
OrganizationDrugs and health products
Recall classType II
What you should doVerify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.Contact the recalling firm if you have any questions about the recall.Report any health product related side effects to Health Canada.Report any other health product safety complaints to Health Canada.

Overview

  • Recalling FirmDrugs and health products
  • Risk LevelType II
Official Agency Alert