FDAFDA · Food and drugs·Recall number D-836-2013
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Published August 14, 2013 · Recall initiated: March 29, 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: reports of small grey/brown particles found in the primary container identified as brass particulates
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 25-037-JT*, Exp 1JAN2015, Note: the lot number may be followed by 01 or 90
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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