FDAFDA · Food and drugs·Recall number D-1073-2019
8.4% Sodium Bicarbonate Injection, USP 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL) 50 mL Single-dose fliptop vial, 25 vials per carton, Rx only Hospira, Inc. Lake Forest, IL 60045 USA ---- NDC 0409-6625-02
Published April 10, 2019 · Recall initiated: March 15, 2019
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; glass particulates
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- United States and Puerto Rico
- Lot
- Lots: 79-238-EV Exp. 1 July 2019; 79-240-EV Exp. 1 July 2019; 80-088-EV Exp. 1 August 2019
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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