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NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actav...

FDA Recall #D-0143-2017 — Class III — October 6, 2016

Recall #D-0143-2017 Date: October 6, 2016 Classification: Class III Status: Terminated

Product Description

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

Reason for Recall

Presence of Foreign Tablets/Capsules

Recalling Firm

Actavis Elizabeth LLC — Elizabeth, NJ

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

27,517 bottles

Distribution

US

Code Information

Lot # 0598B151; Exp 03/18

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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