FDAFDA · Food and drugs·Recall number D-0882-2018
0.9% Sodium Chloride Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7983-02
Published June 27, 2018 · Recall initiated: May 31, 2018
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: Bags have potential to leak.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- ICU Medical Inc
- Distributor
- Nationwide and Canada
- Lot
- Lot #: 85-018-JT, 85-031-JT, Exp. 01/01/2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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