Hospira a Pfizer Company recalls

4 recalls on record · latest: June 15, 2017

Official U.S. recall history for Hospira a Pfizer Company, compiled from official government records.

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Hospira a Pfizer Company recalls 8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, I…

June 15, 2017 · Drug & medication recalls Moderate risk Lack of Sterility Assurance

Hospira a Pfizer Company recalls Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 mL, Single-dose, Caution: Mu…

June 15, 2017 · Drug & medication recalls Moderate risk Lack of Sterility Assurance

Hospira a Pfizer Company recalls Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial cart…

June 15, 2017 · Drug & medication recalls Moderate risk Lack of Sterility Assurance

Hospira a Pfizer Company recalls Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.)…

June 15, 2017 · Drug & medication recalls Moderate risk Lack of Sterility Assurance