# FDA recall D-0404-2015

> **Pfizer Inc.** · Class III · drug recall initiated 2015-02-26.

## Product

Oxecta(TM) (oxycodone HCl) tablets, 7.5 mg, 100 count bottles, Rx only, Manufactured and Distributed by:  King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-526-01

## Reason for recall

Failed Impurities/Degradation Specifications

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0404-2015
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-02-26
- **Report date:** 2015-03-11
- **Termination date:** 2017-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0404-2015

## Citation

> AI Analytics. FDA recall D-0404-2015. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0404-2015. Source: US FDA. Licensed CC0.

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