# FDA recall D-1053-2014

> **Watson Laboratories Inc** · Class II · drug recall initiated 2014-01-15.

## Product

Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only.  Manufactured by Watson Laboratories, Inc., Corona, CA 92880.  Distributed by: Watson Pharma, Inc. NDC: 00591-0517-01.

## Reason for recall

Failed Tablet/Capsule Specifications; Product contains broken tablets.

## Distribution

Nationally in: AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI.

## Key facts

- **Recall number:** D-1053-2014
- **Recalling firm:** Watson Laboratories Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-01-15
- **Report date:** 2014-02-05
- **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-1053-2014

## Citation

> AI Analytics. FDA recall D-1053-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1053-2014. Source: US FDA. Licensed CC0.

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