Viatris recalls Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles,
See all recalls from Viatris →Recalled Product
Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 NDC 0378-3231-93
Hazard / Issue
Failed Impurities/Degradation Specifications; out of specification for Related Compound
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # 3107334, exp. date October 2021
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for Candesartan Cilexetil Tablets, USP →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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