FDAFDA · Food and drugs·Recall number D-851-2013
Ondansetron Injection, USP, 4mg/2mL, (2mg/ml), 2mL single-dose Fliptop Vial, Rx only, Sterile, NDC 0409-4755-03, Hospira, Inc, Lake Forest, IL 60045.
Published August 14, 2013 · Recall initiated: May 20, 2013
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
Presence of Particulate; lot being recalled as a precaution due to the discovery of 2 particles found in a lot which preceded the recalled lot
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ONDANSETRON
- Manufacturer
- Hospira, Inc.
- Distributor
- Nationwide
- Lot
- Lot 25394DK, exp. 01/2015
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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