# FDA recall D-1285-2019

> **Golden State Medical Supply Inc.** · Class II · drug recall initiated 2019-05-01.

## Product

Losartan Potassium Tablets USP 100 mg 90 count bottle NDC 60429-318-90 Rx only GSMS Incorporated

## Reason for recall

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer

## Distribution

IL, MI, MN, PA, TN, TX. Two (2) US government  and one (1) Veterans Affairs accounts. No foreign accounts.

## Key facts

- **Recall number:** D-1285-2019
- **Recalling firm:** Golden State Medical Supply Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-01
- **Report date:** 2019-05-29
- **Termination date:** 2020-02-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Camarillo, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1285-2019

## Citation

> AI Analytics. FDA recall D-1285-2019. Retrieved 2026-06-15 from https://api.ai-analytics.org/recall/D-1285-2019. Source: US FDA. Licensed CC0.

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