PlainRecalls
FDA Drug Low Class III Terminated

Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02

Reported: April 20, 2016 Initiated: March 17, 2016 #D-0821-2016

Product Description

Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp. Date

Details

Recalling Firm
Impax Laboratories, Inc.
Units Affected
42,239 HDPE bottles ( 21,119,500 capsules)
Distribution
Nationwide
Location
Hayward, CA

Frequently Asked Questions

What product was recalled?
Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02. Recalled by Impax Laboratories, Inc.. Units affected: 42,239 HDPE bottles ( 21,119,500 capsules).
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp. Date
Which agency issued this recall?
This recall was issued by the FDA Drug on April 20, 2016. Severity: Low. Recall number: D-0821-2016.