Viatris Inc: Drug Recall

Recall #D-0203-2025 · 12/23/2024

Class II: Risk

Recall Details

Recall Number
D-0203-2025
Classification
Class II
Product Type
Drug
Recalling Firm
Viatris Inc
Status
Terminated
Date Initiated
12/23/2024
Location
Canonsburg, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,215/30 count bottles

Reason for Recall

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

Product Description

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

Distribution Pattern

USA nationwide.

Other Recalls by Viatris Inc

View all recalls by Viatris Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.