FDAFDA · Food and drugs·Recall number D-1359-2016
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Published July 20, 2016 · Recall initiated: June 23, 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
Crystallization: Product contains particulate identified to be crystallized active ingredient.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIAZEPAM
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 52610LL, Exp. 01 OCT 2016; Lot #: 57660LL, Exp. 01 MAR 2017
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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