Recalls / Firms / Hospira a Pfizer Company
Hospira a Pfizer Company
4 FDA drug recalls on record.
| Date | Class | Drug | Status |
|---|---|---|---|
| 2017-06-15 | Class II | 8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL | Terminated |
| 2017-06-15 | Class II | Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 04 | Terminated |
| 2017-06-15 | Class II | Quelicin | Terminated |
| 2017-06-15 | Class II | Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 | Terminated |