FDAFDA · Food and drugs·Recall number D-0831-2016
Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-7715-02, Barcode (01) 0 030409 771502 2
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# 52-031-JT, Exp 10/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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