FDAFDA · Food and drugs·Recall number D-0865-2016
8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02
Published June 1, 2016 · Recall initiated: March 18, 2016
Status when published: Ongoing — 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: particulate matter identified as an insect in one vial.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot # 56-148-EV, Exp 8/1/2017
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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