# FDA recall D-1572-2014

> **Qualitest Pharmaceuticals** · Class II · drug recall initiated 2014-08-27.

## Product

OXYCODONE and ACETAMINOPHEN, USP 10 mg/325 mg, CII, 100 TABLETS, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-4982-21

## Reason for recall

Failed Tablet/Capsule Specifications: Broken tablets found in sealed bottles.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1572-2014
- **Recalling firm:** Qualitest Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-08-27
- **Report date:** 2014-09-10
- **Termination date:** 2016-02-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Huntsville, AL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1572-2014

## Citation

> AI Analytics. FDA recall D-1572-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1572-2014. Source: US FDA. Licensed CC0.

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