FDAFDA · Food and drugs·Recall number D-0820-2016
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
Published April 20, 2016 · Recall initiated: March 17, 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
Labeling: Incorrect or Missing Lot and/or Exp. Date
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Impax Laboratories, Inc.
- Distributor
- Nationwide
- Lot
- Lot # 10008624, 10008831; Exp. 10/16 Lot # 10009339; Exp. 02/17 Lot # 10009566,10009627; Exp. 04/17 Lot # 10010200, 20001419A, 20001426A; Exp. 10/17 Lot # 20001732A; Exp. 04/18 Lot # 20001790A, 20001791A, 20001792A; Exp. 05/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States