FDAFDA · Food and drugs·Recall number D-1036-2014
Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.
Published February 5, 2014 · Recall initiated: January 9, 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
Lack of Assurance of Sterility; potential leakage from administrative port.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide including Puerto Rico
- Lot
- Lot #: 26-125-JT, Exp: 8/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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