US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 17, 2013 (13 years ago)

Enablex (darifenacin) Extended Release Tablet, 15 mg per tablet. Physician Sample 7…

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

Why it was recalled

Failed Impurities/Degradation Specifications: unspecified degradation product

What was recalled

Enablex (darifenacin) Extended Release Tablet, 15 mg per tablet. Physician Sample 7 Tablets bottle, Rx only, Mfd by: Novartis Pharma Stein AG, Stein, Switzerland, NDC 0078-9420-07

Recalling firm
Warner Chilcott US LLC
NDC code
0078-9420-07
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-822-2013

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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