# FDA recall D-66251-001

> **Watson Laboratories Inc** · Class II · drug recall initiated 2013-09-13.

## Product

Oxycodone and Acetaminophen Tablets, USP 10 mg/650 mg, CII, 100 Count Bottles, Rx Only, Manufactured by: Watson Laboratories, Inc. Corona, CA 92880 USA, NDC 0591-0825-01

## Reason for recall

Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500 mg were found in a sealed 100 count bottle of Oxycodone and Acetaminophen Tablets, USP 10/650 mg lot# 705791A.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-66251-001
- **Recalling firm:** Watson Laboratories Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-09-13
- **Report date:** 2013-10-09
- **Termination date:** 2014-07-25

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-66251-001

## Citation

> AI Analytics. FDA recall D-66251-001. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-66251-001. Source: US FDA. Licensed CC0.

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