# FDA recall D-1279-2014

> **Legacy Pharmaceutical Packaging** · Class II · drug recall initiated 2014-02-14.

## Product

Fluoxetine Capsules, USP, 20 mg, 30-count bottles, Rx only, Distributed by: Wal-Mart, Bentonville, AR  72716; Manufactured by: TEVA PHARMACEUTICALS USA, Sellersville, PA  18960; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO  63045, NDC 68645-130-54, UPC 3 68645 13054 5.

## Reason for recall

Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1279-2014
- **Recalling firm:** Legacy Pharmaceutical Packaging
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-02-14
- **Report date:** 2014-05-07
- **Termination date:** 2017-11-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Earth City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1279-2014

## Citation

> AI Analytics. FDA recall D-1279-2014. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-1279-2014. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
