FDAApril 7, 2015drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

hospira

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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