FDAFDA · Food and drugs·Recall number D-262-2013
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
Published April 24, 2013 · Recall initiated: January 25, 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
Non-Sterility: Confirmed customer complaint of product contaminated with mold.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 05-019-JT*, Exp 05/01/13; lot number * may be followed by 01, 90, or 91.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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