FDAFDA · Food and drugs·Recall number D-0976-2015
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
Published May 13, 2015 · Recall initiated: March 5, 2015
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 Matter: Confirmed finding of human hair floating in IV solution.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide.
- Lot
- Lot # 45-110-C6; Exp 03/1/16
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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