FDAFDA · Food and drugs·Recall number D-1425-2014
Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62
Published July 16, 2014 · Recall initiated: June 6, 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: Confirmed consumer report of fluid leaking from primary container of bag.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM AND DEXTROSE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot # 34-811-KL, 36-106-KL, 36-114-KL; Exp. 12/15; 36-101-KL, Exp. 12/15; 37-202-KL, Exp. 1/16; 38-302-KL, Exp. 2/16; 38-305-KL, Exp. 2/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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