Hospira Inc. recalls Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, H
See all recalls from Hospira Inc. →Recalled Product
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Hazard / Issue
Crystallization: Product contains particulate identified to be crystallized active ingredient.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 52610LL, Exp. 01 OCT 2016; Lot #: 57660LL, Exp. 01 MAR 2017
✅ 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 Diazepam Injection USP 10mg/2mL →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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