FDADecember 22, 2014drug

0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11

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

The hazard

Lack of Assurance of Sterility: The product has the potential for solution 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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