Cardura XL (doxazosin) extended release tablets 8mg, 30-count bottles, Rx Only Made in Singapore, Distributed by Roerig
Summary
The FDA issued a Class II for Cardura XL (doxazosin) extended release tablets 8mg, 30-count bottles, Rx Only M by Viatris Inc. Reason: Failed Impurities/Degradation Specifications.
Details
Source
Drug Recall
External ID
D-0603-2024
Action Date
2024-07-24
Status
Completed
Category
drug
Product Description
Cardura XL (doxazosin) extended release tablets 8mg, 30-count bottles, Rx Only Made in Singapore, Distributed by Roerig Division of Pfizer Inc, NY, NY 10017 NDC 0049-2080-10
Lot/Code Info: Lot#: 8147041; Exp. June 2024 Lot#: 8163765; Exp. March 2025
Quantity Affected: 3,694 bottles
Reason for Recall
Failed Impurities/Degradation Specifications
Distribution
U.S. Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-30
Company
Canonsburg, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 41 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Viatris Inc has 23 FDA actions in our database, including 23 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Viatris Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Viatris Inc have FDA actions?
Viatris Inc has 23 FDA actions in our database, including 23 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0603-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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