US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 23, 2024 (2 years ago)

Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.

What was recalled

Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-078-93

Recalling firm
Viatris Inc
NDC code
58151-078-93
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0204-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Doxazosin recalls

See all