Hospira a Pfizer Company
Rocky Mount, NC, United States
4
Total Recalls
0
Class I Recalls
0
Ongoing Recalls
Recalls by Hospira a Pfizer Company
FDA Drug
Class II
Terminated
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, INC, Lake Forest, IL 60045 USA, NDC: 0409-6625-02
June 15, 2017
Hospira a Pfizer Company
91,483,150 50 mL single dose vials units
FDA Drug
Class II
Terminated
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
June 15, 2017
Hospira a Pfizer Company
20,337,650 15 mL single dose vials units
FDA Drug
Class II
Terminated
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
June 15, 2017
Hospira a Pfizer Company
21,436,700 5mL single dose vials units
FDA Drug
Class II
Terminated
Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02), b.) 25 vial carton (NDC: 0409-6629-25).
June 15, 2017
Hospira a Pfizer Company
15,034,600 10 mL multiple dose use vials units