US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 6, 2016 (10 years ago)

NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Presence of Foreign Tablets/Capsules

What was recalled

NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-2407-10

Recalling firm
Actavis Elizabeth LLC
NDC code
0228-2407-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0143-2017

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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