Viatris recalls Cardura XL 4mg extended-release tablets due to impurity issues found during stability testing. This affects specific lot numbers and requires patient consultation with healthcare providers.
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Viatris has recalled Cardura XL 4mg extended-release tablets because stability testing detected impurities that could affect safety. Patients should consult their healthcare provider before using these tablets.
Stability testing found impurities in the medication that could potentially affect safety. This issue was identified during quality control checks but does not indicate immediate harm to users.
Patients prescribed Cardura XL 4mg extended-release tablets by a healthcare provider. Those with specific lot numbers are most at risk.
Check for the 4mg extended-release tablets in a 30-count bottle with lot number 8182298, expiring October 31, 2025. The product is prescription-only and distributed by Viatris Specialty LLC.
Patients should contact their healthcare provider before using the recalled medication to discuss alternatives.
The recall indicates impurities were found during stability testing, but the product is not considered unsafe for immediate use. Patients should consult their healthcare provider.
Lot number 8182298, expiring October 31, 2025.
Check for the 4mg extended-release tablets in a 30-count bottle with lot number 8182298, expiring October 31, 2025.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0204-2025 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0204-2025 from Viatris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
