Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, M…

Recall date

December 23, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0203-2025

FDA classification

Class II

Brand / firm

Viatris Inc

Sold / distributed

USA nationwide.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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