FDAJune 15, 2017drug

Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 mL, Single-dose, Caution: Must Be Diluted, Rx Only, Mfd by Hospira, Inc. Lake Forest, IL 60045 USA, NDC: 0409-7295-01

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

The hazard

Lack of Sterility Assurance

What to do

FDA enforcement status: Terminated

Brands named

hospira a pfizerhospira

Recall history

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

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