FDAFDA · Food and drugs·Recall number D-0095-2023
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
Published January 11, 2023 · Recall initiated: December 28, 2022
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ACYCLOVIR SODIUM
- Manufacturer
- Eugia US LLC
- Distributor
- Nationwide in the USA
- UPC
- 0355150155200
- Lot
- Lot # AC22004, Expiry: 08/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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