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
Reported: June 1, 2016 Initiated: March 18, 2016 #D-0865-2016
Product Description
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
Reason for Recall
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 72,000 units
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Hospira Inc.. Units affected: 72,000 units.
Why was this product recalled? ▼
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 1, 2016. Severity: Critical. Recall number: D-0865-2016.
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