Class II · Moderate riskOngoing 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.
Reason Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.