FDAFDA · Food and drugs·Recall number D-0324-2015
HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7620-03
Published December 31, 2014 · Recall initiated: September 11, 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: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 41-046-JT, Exp 11/01/2015
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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