FDAFDA · Food and drugs·Recall number D-0143-2017
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
Published November 30, 2016 · Recall initiated: October 6, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Tablets/Capsules
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Actavis Elizabeth LLC
- Distributor
- US
- Lot
- Lot # 0598B151; Exp 03/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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