# FDA recall D-0820-2016

> **Impax Laboratories, Inc.** · Class III · drug recall initiated 2016-03-17.

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0820-2016
- **Recalling firm:** Impax Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-03-17
- **Report date:** 2016-04-20
- **Termination date:** 2016-10-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hayward, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0820-2016

## Citation

> AI Analytics. FDA recall D-0820-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0820-2016. Source: US FDA. Licensed CC0.

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