# FDA recall D-0624-2024

> **Eugia US LLC** · Class II · drug recall initiated 2024-07-26.

## Product

Progesterone Injection, USP, 500 mg 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: Complaint received of a glass particle in the vial.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0624-2024
- **Recalling firm:** Eugia US LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-07-26
- **Report date:** 2024-08-07

- **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-0624-2024

## Citation

> AI Analytics. FDA recall D-0624-2024. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/D-0624-2024. Source: US FDA. Licensed CC0.

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