# FDA recall D-0822-2016

> **Amerisource Health Services** · Class III · drug recall initiated 2016-03-31.

## Product

Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217, Carton of 20: NDC 68084-835-32, Individual Dose: NDC 68084-835-33.

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0822-2016
- **Recalling firm:** Amerisource Health Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-03-31
- **Report date:** 2016-04-20
- **Termination date:** 2017-01-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbus, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0822-2016

## Citation

> AI Analytics. FDA recall D-0822-2016. Retrieved 2026-05-23 from https://api.ai-analytics.org/recall/D-0822-2016. Source: US FDA. Licensed CC0.

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