Recalls / Active ingredient / Sodium Acetate Anhydrous
Sodium Acetate Anhydrous
1 FDA drug recall involving the active ingredient “Sodium Acetate Anhydrous”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2013-02-26 | Class II | Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE | Hospira Inc. |