# FDA recall D-018-2014

> **Actavis Elizabeth LLC** · Class II · drug recall initiated 2013-10-09.

## Product

Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-4025-11

## Reason for recall

Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets

## Distribution

Nationwide

## Key facts

- **Recall number:** D-018-2014
- **Recalling firm:** Actavis Elizabeth LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-10-09
- **Report date:** 2013-12-04
- **Termination date:** 2014-11-03

- **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-018-2014

## Citation

> AI Analytics. FDA recall D-018-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-018-2014. Source: US FDA. Licensed CC0.

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