Fresenius Kabi Vancomycin HCl Recall: Lack of Sterility Risk

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Contact the company & request your remedy

Recalling firmFresenius Kabi Compounding, LLC20 Dan Rd, N/A · Canton, MA 02021-2809

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Fresenius Kabi is recalling certain vancomycin HCl injections that may not be sterile, posing infection risks. Patients should not use these products.

Why it’s dangerous

The injections lack assurance of sterility, meaning they could contain harmful bacteria or contaminants. If used, this could lead to serious infections or health complications.

Who’s affected

Healthcare providers and patients using the recalled vancomycin HCl injections for medical treatment. Those with the specific lot numbers are most at risk.

How to tell if you have this one

Check the product label for the lot numbers C274-000047611 (expires Feb 2026) or C274-000049633 (expires May 2026). The product is a vancomycin HCl injection for medical use.

Brand
Fresenius Kabi
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop Using Now
Immediately stop using the recalled vancomycin HCl injections if you have them.

✎ GovInfoNow

Questions people ask

What is the specific product being recalled?

Vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, with lot numbers C274-000047611 or C274-000049633.

How can I check if my product is affected?

Check the product label for the lot numbers C274-000047611 (expires Feb 2026) or C274-000049633 (expires May 2026).

What should I do if I have the recalled product?

Immediately stop using it and contact Fresenius Kabi for further instructions.

Take action

Contact Fresenius Kabi

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

✉️ Open in email

Subject: Recall D-0337-2026 — Fresenius Kabi Fresenius Kabi

Hello,

I own a Fresenius Kabi that is covered by recall D-0337-2026 from Fresenius Kabi.

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.

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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-0337-2026 (February 5, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0337-2026 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.

Fresenius Kabi Compounding, LLC recalls vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan

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