FDAFDA · Food and drugs·Recall number D-0827-2016
Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7918-19, Barcode (01) 0 030409 791819 5
Published April 27, 2016 · Recall initiated: March 8, 2016
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
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- US: Nationwide and Singapore
- Lot
- Lot# 48-010-JT, Exp 12/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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