Data Composite

Recall D-0489-2025

US Class II Ongoing · initiated 2025-05-28

Recalling firm

Pfizer Inc., NY

Product

DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of 10 Fliptop Vials, Rx only, For Intravenous Use Only, Made in Italy, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. NDC Carton: 0409-2344-02; NDC Vial: 0409-2344-62

Reason for recall

Discoloration; discolored solution from cracked vials

← All recalls