US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 25, 2024 (2 years ago)

NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 8 mg per 250 mL, Single…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP violations

What was recalled

NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 8 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-027-58

Recalling firm
Fresenius Kabi Compounding, LLC
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0020-2025

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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