FDAFDA · Food and drugs·Recall number D-013-2014
Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL Single-dose Vial, Rx Only, Sterile, Hospira Inc., Lake Forest IL 60045, USA, NDC 0409-4755-03
Published November 27, 2013 · Recall initiated: September 24, 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 Particular Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ONDANSETRON
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- UPC
- 040947550329
- Lot
- 29-484-DK* and 29-510-DK* Exp 05/01/2015 (lot number may be proceeded with an 01)
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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