FDAFDA · Food and drugs·Recall number D-608-2013
0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02
Published June 26, 2013 · Recall initiated: June 6, 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: The product has the potential for solution to leak at or near the administrative port of the primary container.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot #: 16-031-JT*, Exp 1APR2014; Note the * may be followed by 01 or 02
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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