RecallDepth
Class II Terminated

DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted Prior to Use, (12.5 mg per mL), Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2025-20

Company
Hospira Inc.
Recall Initiated
August 15, 2016
Posted
September 21, 2016
Recall Number
D-1500-2016
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
24000 vials
Firm Location
Lake Forest, IL, United States

Reason for Recall

Discoloration: Firm received complaints of product discoloration and particulates.

Distribution

Product was distributed nationwide. 23700 units distributed to US and Puerto Rico, and Bahamas was 300 units. 30 units returned by customer and destroyed internally.

Lot / Code Info

Lot #: 52175DD, Exp 01 Oct 2016

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