# FDA recall D-0891-2022

> **Preferred Pharmaceuticals, Inc.** · Class II · drug recall initiated 2022-05-03.

## Product

Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.

## Reason for recall

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

## Distribution

Within the U.S in FL and CA.

## Key facts

- **Recall number:** D-0891-2022
- **Recalling firm:** Preferred Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-05-03
- **Report date:** 2022-06-01
- **Termination date:** 2022-09-21

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0891-2022

## Citation

> AI Analytics. FDA recall D-0891-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-0891-2022. Source: US FDA. Licensed CC0.

---

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