Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-cou
See all recalls from Viatris Inc →Recalled Product
Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-079-93
Hazard / Issue
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # 8181625, Exp 12/31/2025
✅ 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.
Looking for a safe alternative?
Search Amazon for Cardura XL (doxazosin) extended →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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