FDAFDA · Food and drugs·Recall number D-0969-2015
0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02
Published April 29, 2015 · Recall initiated: January 20, 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; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 44-002-JT (the lot number may be followed by 01 to 99), Exp 08/01/2016
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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