FDAMarch 23, 2016drug

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

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

The hazard

Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.

What to do

FDA enforcement status: Ongoing

Brands named

hospira

UPCs

20304092168025

Recall history

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

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