# FDA recall D-1434-2012

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2012-04-09.

## Product

Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg,  500 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-340-05

## Reason for recall

Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1434-2012
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-04-09
- **Report date:** 2012-08-08
- **Termination date:** 2013-01-24

- **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-1434-2012

## Citation

> AI Analytics. FDA recall D-1434-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1434-2012. Source: US FDA. Licensed CC0.

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