US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 7, 2015 (11 years ago)

0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by…

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

Why it was recalled

Lack of Sterility Assurance: The product has the potential to leak at the administrative port.

What was recalled

0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 60045, NDC: 0409-7101-67

Recalling firm
Hospira Inc.
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0490-2015

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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