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High risk Drugs & MedicationsClass II

Fresenius Kabi Vancomycin Recall

Vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA

Updated February 5, 2026

Fresenius Kabi Compounding is recalling vancomycin HCl in 0.9% Sodium Chloride Injection because the manufacturer cannot ensure the product is sterile. Patients receiving non-sterile injected medications face serious risk of infection.

Is the Fresenius Kabi Compounding, LLC recalled? Yes. This product was recalled by FDA on February 5, 2026. Details below.

What is recalled

Vancomycin HCl, 1.5 grams, added to 500 mL 0.9% Sodium Chloride Injection, USP. NDC: 71506-016-59. Manufactured by Fagron Sterile Services, 20 Dan Road, Canton, MA 02021.

Am I affected

You are affected if you received an IV injection of vancomycin in 0.9% Sodium Chloride Injection with NDC 71506-016-59 from Fagron Sterile Services. Check with your healthcare provider or pharmacy about any doses administered.

What to do right now

Contact your healthcare provider immediately if you received this injection. Do not use any remaining doses of this product. Your provider will advise whether you need evaluation for signs of infection.

The hazard

Lack of Assurance of Sterility

Brands affected

Fresenius Kabi Compounding, LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0336-2026
Classification
Class II
Recalled
February 5, 2026
Read the official notice

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