US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 22, 2014 (13 years ago)

Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV…

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

Why it was recalled

Subpotent; 18 month time point

What was recalled

Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11, 25 vials in tray, each boxed vial individually labeled as: Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11.

Recalling firm
Fresenius Kabi USA, LLC
NDC code
63323-540-11
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1148-2014

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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