Impax Laboratories, Inc. recalls Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, N
Recalled April 20, 2016 · FDA recall D-0820-2016 · Impax Laboratories
Hazard
Labeling: Incorrect or Missing Lot and/or Exp. Date · FDA Class III
Units
28,001 HDPE bottles (14,000,500 capsules)
Sold at
Nationwide
Description
Labeling: Incorrect or Missing Lot and/or Exp. Date
Product
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
Manufacturer(s)
Impax Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →