FDAFDA · Food and drugs·Recall number D-1540-2014
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
Published August 27, 2014 · Recall initiated: January 10, 2014
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
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DOBUTAMINE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico.
- Lot
- Lot # 27-352-DK; Exp 03/15
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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