8.4% Sodium Bicarbonate Injection recall: Particulate Matter
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
Why was 8.4% Sodium Bicarbonate Injection recalled?
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 56-148-EV, Exp 8/1/2017
- Product
- 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
- Recalling firm
- Hospira Inc.
- Quantity
- 72,000 units
- Distribution
- Nationwide
- Recall date
- June 1, 2016
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)