# FDA recall D-0253-2015

> **Micro Labs Usa, Inc                                    S** · Class II · drug recall initiated 2014-09-22.

## Product

LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles, Rx Only. Manufactured by: Micro Labs Limited, Goa-403 722, INDIA. Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540. NDC 42571-110-10

## Reason for recall

Failed Content Uniformity Specifications; Dry mix failed blend uniformity.

## Distribution

U.S. Including: New York

## Key facts

- **Recall number:** D-0253-2015
- **Recalling firm:** Micro Labs Usa, Inc                                    S
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-09-22
- **Report date:** 2014-11-26
- **Termination date:** 2015-12-22

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0253-2015

## Citation

> AI Analytics. FDA recall D-0253-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0253-2015. Source: US FDA. Licensed CC0.

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