Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to Failed Dissolution Specifications: Drug failed stage III dissolution...
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 Forest Pharmaceuticals Inc directly.
Affected Products
Bystolic (nebivolol) tablets, 20 mg/tablet. 7 Tablet Professional Sample Bottle, Rx Only. Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, Missouri 63045. NDC 0456-1420-07.
Quantity: 92,544 Bottles
Why Was This Recalled?
Failed Dissolution Specifications: Drug failed stage III dissolution testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Forest Pharmaceuticals Inc
Forest Pharmaceuticals Inc has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report