Sagent Oxacillin Injection Recall: Risk of Contamination

Take action

Contact the company & request your remedy

Recalling firmSagent Pharmaceuticals1901 N Roselle Rd Ste 450, N/A · Schaumburg, IL 60195-3194

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Sagent Pharmaceuticals is recalling Oxacillin for Injection, USP, 10 gram bulk packages because they may not be sterile. This could lead to infections if used in medical treatments.

Why it’s dangerous

The product may not be sterile, which could cause infections during intravenous administration. This is a serious risk for patients receiving the medication through medical procedures.

Who’s affected

Healthcare providers using the recalled Oxacillin for IV treatments in the US. Patients receiving this medication through a pharmacy are at risk if they use contaminated products.

How to tell if you have this one

Check for NDC numbers 25021-163-99 (lot OXT202/OXT203/OXT301) or 25021-163-68 (lot OXT205/OXT204). Products made in India with expiration dates through May 2025.

Brand
Sagent Pharmaceuticals
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for NDC numbers 25021-163-99 or 25021-163-68 on the bottle label.
Contact Pharmacy
Ask your pharmacy if they have the recalled lots and request a replacement or refund.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may not be sterile, which could cause infections. Do not use until the recall is resolved.

What lots are affected?

Lots OXT202, OXT203, OXT301 (expiring May 31, 2025) and OXT205, OXT204 (expiring May 31, 2025).

How do I know if I have the recalled product?

Check for NDC numbers 25021-163-99 or 25021-163-68 on the bottle label.

Take action

Contact Sagent Pharmaceuticals

We’ve drafted a message you can send Sagent Pharmaceuticals to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0937-2023 — Sagent Pharmaceuticals Sagent Pharmaceuticals

Hello,

I own a Sagent Pharmaceuticals that is covered by recall D-0937-2023 from Sagent Pharmaceuticals.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0937-2023 (July 11, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0937-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Sagent Pharmaceuticals recalls Oxacillin for Injection, USP, 10 gram per pharmacy Bulk Package bottle, For Intravenous Use, Rx only, packaged as a)

Recall notice