# FDA recall D-0095-2023

> **Eugia US LLC** · Class II · drug recall initiated 2022-12-28.

## Product

Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx only,  Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd, E. Windsor, NJ 08520; Made in India. NDC 55150-155-20

## Reason for recall

Presence of Particulate Matter: Customer complaint of dark particles found inside the vial

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0095-2023
- **Recalling firm:** Eugia US LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2022-12-28
- **Report date:** 2023-01-11

- **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-0095-2023

## Citation

> AI Analytics. FDA recall D-0095-2023. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/D-0095-2023. Source: US FDA. Licensed CC0.

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