# FDA recall D-1500-2014

> **Jubilant Cadista Pharmaceuticals Inc.** · Class II · drug recall initiated 2014-07-11.

## Product

Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90

## Reason for recall

Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1500-2014
- **Recalling firm:** Jubilant Cadista Pharmaceuticals Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-11
- **Report date:** 2014-08-06
- **Termination date:** 2016-09-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salisbury, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1500-2014

## Citation

> AI Analytics. FDA recall D-1500-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1500-2014. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*