drugs Class I Updated 2014-08-27

Hospira Inc. recalls DOBUTamine Injection, USP, 250 mg per 20 mL, 20 mL Single-do

Recalled Product

DOBUTamine Injection, USP, 250 mg per 20 mL, 20 mL Single-dose Fliptop Vial, Rx only, Manufactured for Hospira Inc., Lake Forest, IL 60045 USA. NDC 0409-2344-02

Hazard / Issue

Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # 27-352-DK; Exp 03/15
View official government recall

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