US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 27, 2018 (8 years ago)

Levetiracetam in 0.75% Sodium Chloride Injection

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

Why it was recalled

Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

What was recalled

Levetiracetam in 0.75% Sodium Chloride Injection, 1000 mg per 100 mL (10 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-247-47.

Recalling firm
AuroMedics Pharma LLC
NDC code
55150-247-47
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0706-2018

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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