FDAFDA · Food and drugs·Recall number D-183-2013
0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,
Published March 13, 2013 · Recall initiated: January 8, 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 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 Number 02-117-JT Exp. 02/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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