Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed Impurities/Degradation Specifications; out of specification for Related...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris directly.
Affected Products
Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 NDC 0378-3231-93
Quantity: 21,094
Why Was This Recalled?
Failed Impurities/Degradation Specifications; out of specification for Related Compound
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris
Viatris has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report