US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 11, 2023 (3 years ago)

Oxacillin for Injection, USP, 10 gram per pharmacy Bulk Package bottle, For Intravenous…

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

Why it was recalled

Lack of Assurance of Sterility

What was recalled

Oxacillin for Injection, USP, 10 gram per pharmacy Bulk Package bottle, For Intravenous Use, Rx only, packaged as a) NDC 25021-163-99 and b) novaplus NDC 25021-163-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

Recalling firm
Sagent Pharmaceuticals
NDC code
25021-163-99
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0937-2023

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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