Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Carvedilol Tablets Recalled by Viatris Inc Due to Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.
Affected Products
Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC 0378-3634-05
Quantity: 2,794 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris Inc
Viatris Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report