FDAFDA · Food and drugs·Recall number D-0480-2017
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Published March 1, 2017 · Recall initiated: February 10, 2017
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
Lack of Sterility Assurance: customer report of leaking bag
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc., A Pfizer Company
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot: 54-054-JT, 6/1/2017
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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