Taro-candesartan: Affected Lots Were Manufactured Using An Active Ingredient That Was Out Of Specification For Dissolution

Certain batches of TARO-CANDESARTAN tablets have been recalled in Canada because the active ingredient in these batches doesn't meet the required dissolution specifications, meaning it may not break down properly in the body. This is a Class I recall, which indicates a serious quality issue. The affected product was distributed across Canada.

Product
TARO-CANDESARTAN
Reason
Product quality concern
Classification
Class II
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2026-02-09
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/daa00c77-4acd-4a26-90bd-5f01fd44d57b