US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Dec 28, 2022 (4 years ago)

Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Eugia US LLC
NDC code
55150-155-20
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0095-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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