# FDA recall D-1061-2013

> **Watson Laboratories Inc** · Class III · drug recall initiated 2013-08-30.

## Product

Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.

## Reason for recall

Defective Container:  Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1061-2013
- **Recalling firm:** Watson Laboratories Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-08-30
- **Report date:** 2013-09-25
- **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-1061-2013

## Citation

> AI Analytics. FDA recall D-1061-2013. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1061-2013. Source: US FDA. Licensed CC0.

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