US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 9, 2014 (13 years ago)

Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium…

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

Why it was recalled

Lack of Assurance of Sterility; potential leakage from administrative port.

What was recalled

Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.

Recalling firm
Hospira Inc.
NDC code
0409-7620-59
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1036-2014

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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