FDAMarch 5, 2015drug

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

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

The hazard

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

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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