FDAAugust 25, 2015drug

1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02

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

The hazard

Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.

What to do

FDA enforcement status: Ongoing

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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