FDAFDA · Food and drugs·Recall number D-502-2013
DOBUTamine in 5% Dextrose Injection, USP, 250 mg Total, 1000 mcg/mL 250 mL bag, Rx only, HOPIRA, INC., LAKE FOREST, IL 60045 NDC 0409-2346-32
Published June 12, 2013 · Recall initiated: April 30, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Confirmed report of leaking in the primary container.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DOBUTAMINE IN DEXTROSE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot 11-309-KL
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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