# FDA recall D-0363-2025

> **Eugia US LLC** · Class II · drug recall initiated 2025-04-10.

## Product

Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial,  Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, India, NDC 55150-277-01

## Reason for recall

cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.

## Distribution

Nationwide USA

## Key facts

- **Recall number:** D-0363-2025
- **Recalling firm:** Eugia US LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-04-10
- **Report date:** 2025-04-23

- **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-0363-2025

## Citation

> AI Analytics. FDA recall D-0363-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/D-0363-2025. Source: US FDA. Licensed CC0.

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