FDA recall D-0143-2017
Actavis Elizabeth LLC · Class III · drug
Product
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
Distribution
US
Key facts
- Status
- Terminated
- Initiation date
- 2016-10-06
- Report date
- 2016-11-30
- Termination date
- 2017-05-08
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Elizabeth, NJ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0143-2017