# FDA recall D-180-2013

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2012-08-01.

## Product

Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli,  India 502 325, NDC 55111-344-30

## Reason for recall

Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-180-2013
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-08-01
- **Report date:** 2013-03-06
- **Termination date:** 2013-05-24

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-180-2013

## Citation

> AI Analytics. FDA recall D-180-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-180-2013. Source: US FDA. Licensed CC0.

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