US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Feb 5, 2026 (7 months ago)

thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron…

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

thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-079-56.

Recalling firm
Fresenius Kabi Compounding, LLC
NDC code
71506-079-56
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0335-2026

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.

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