US Drug Recall Register
Class I · High risk Ongoing Initiated Mar 18, 2016 (10 years ago)

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: particulate matter identified as an insect in one vial.

What 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

Recalling firm
Hospira Inc.
NDC code
0409-6625-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0865-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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