PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: November 30, 2016 Initiated: October 6, 2016 #D-0143-2017

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

Details

Recalling Firm
Actavis Elizabeth LLC
Units Affected
27,517 bottles
Distribution
US
Location
Elizabeth, NJ

Frequently Asked Questions

What product 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. Recalled by Actavis Elizabeth LLC. Units affected: 27,517 bottles.
Why was this product recalled?
Presence of Foreign Tablets/Capsules
Which agency issued this recall?
This recall was issued by the FDA Drug on November 30, 2016. Severity: Low. Recall number: D-0143-2017.