US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 19, 2014 (12 years ago)

Bystolic (nebivolol) tablets, 20 mg/tablet. 7 Tablet Professional Sample Bottle, Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Dissolution Specifications: Drug failed stage III dissolution testing.

What was recalled

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.

Recalling firm
Forest Pharmaceuticals Inc
NDC code
0456-1420-07
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1412-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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