US Drug Recall Register
Class I · High risk Terminated Initiated Oct 4, 2022 (4 years ago)

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials…

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

Why it was recalled

Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration

What was recalled

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Distributed by: Exela Pharma Sciences, LLC Lenoir, NC 28645. Carton NDC 51754-5001-5, vial NDC 51754-5001-1

Recalling firm
Exela Pharma Sciences LLC
NDC code
51754-5001-5
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0022-2023

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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