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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