# FDA recall D-0186-2025

> **Eugia US LLC** · Class II · drug recall initiated 2024-12-27.

## Product

Progesterone Injection USP, 500mg per 10 mL (50mg/mL), 10 mL Multiple Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor NJ 08520  NDC # 55150-306-10

## Reason for recall

Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.

## Distribution

Distributed Nationwide in the USA.

## Key facts

- **Recall number:** D-0186-2025
- **Recalling firm:** Eugia US LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-12-27
- **Report date:** 2025-01-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0186-2025

## Citation

> AI Analytics. FDA recall D-0186-2025. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0186-2025. Source: US FDA. Licensed CC0.

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