# FDA recall D-0161-2016

> **Pfizer Inc.** · Class II · drug recall initiated 2015-09-24.

## Product

Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of Pfizer Inc, NY, NY 10017, NDC 0009-0029-01

## Reason for recall

Subpotent Drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0161-2016
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-09-24
- **Report date:** 2015-11-04
- **Termination date:** 2017-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0161-2016

## Citation

> AI Analytics. FDA recall D-0161-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0161-2016. Source: US FDA. Licensed CC0.

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