FDAFDA · Food and drugs·Recall number D-922-2013
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Published September 4, 2013 · Recall initiated: August 31, 2012
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; product may contain fibrous material
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot Number 05-201-JT, Expiration Date 1MAY2013
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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