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Apo-candesartan: affected lots were manufactured using an active ingredient that was out of specification for dissolution
Official notice
16 Feb 2026
Last checked
16 Feb 2026
An official Health Canada notice concerns Apo-candesartan: affected lots were manufactured using an active ingredient that was out of specification for dissolution. Affected lots were manufactured using an active ingredient that was out of specification for dissolution. Published 2026-02-16.
What to do now
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.
Recall number
81606
Official notice
2026-02-16
The hazard
The hazard
Affected lots were manufactured using an active ingredient that was out of specification for dissolution.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Lots
Other
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Product 2
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand
Manufacturer
Phone
Brand: Apotex. Contact: the recalling firm if you have any questions about the recall.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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