FDAFDA · Food and drugs·Recall number D-263-2013
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09.
Published April 24, 2013 · Recall initiated: October 5, 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
Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot # :12-160-JT*, Exp 12/01/13; lot number * may be followed by 01 or 90
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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