Hospira Inc. recalls Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL B
See all recalls from Hospira Inc. →Recalled Product
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
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# 52-031-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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Search Amazon for Mannitol I.V., 20%, USP →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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