FDAFDA · Food and drugs·Recall number D-206-2013
METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)
Published March 27, 2013 · Recall initiated: February 15, 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
Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide.
- Lot
- Lot code 12-074-JT Exp 12/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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