FDAFDA · Food and drugs·Recall number D-813-2013
Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-4888-20.
Published July 31, 2013 · Recall initiated: June 27, 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
Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM CHLORIDE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Guam
- Lot
- Lot #: 15-058-DK*, Exp 1MAR2014; note the * may be followed by 01
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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