Impax Laboratories, Inc. Recall: Fenofibrate Capsules (Micronized) 134 mg, 500-count bottl
Impax Laboratories, Inc. Recall: Fenofibrate Capsules (Micronized) 134 mg, 500-count bottl is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Impax Laboratories, Inc.; Product: Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA
| Recalling firm | Impax Laboratories, Inc. |
|---|---|
| Product | Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02 |
| Reason for recall | Labeling: Incorrect or Missing Lot and/or Exp. Date |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20160317 |
| Recall number | D-0820-2016 |
| Category | drug |
| State | CA |
| Country | United States |
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