Hospira Inc. recalls Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL
See all recalls from Hospira Inc. →Recalled Product
Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2
Hazard / Issue
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot# 52-114-JT, Exp 10/16
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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