# FDA recall D-1091-2014

> **Actavis Elizabeth LLC** · Class II · drug recall initiated 2014-02-04.

## Product

Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only,  Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3 0228-3086-06 2.

## Reason for recall

Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1091-2014
- **Recalling firm:** Actavis Elizabeth LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-02-04
- **Report date:** 2014-03-12
- **Termination date:** 2015-01-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Elizabeth, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1091-2014

## Citation

> AI Analytics. FDA recall D-1091-2014. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1091-2014. Source: US FDA. Licensed CC0.

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