FDA recall record

Sagent Pharmaceuticals Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use recall — FDA D-0936-2023

Lack of Assurance of Sterility

Class IIclassification
D-0936-2023official record ID
Aug 2, 2023report date

Recall record at a glance

Official recordD-0936-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSagent Pharmaceuticals
Report dateAug 2, 2023
Recall initiation dateJul 11, 2023
Quantity65,710 vials for 1 g and 2 g strength
LocationSchaumburg, IL, United States

Official product description

Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use, Rx only, labeled as a) NDC 25021-162-24 and b) novaplus NDC 25021-162-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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