Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Sodium Bicarbonate 8.4% Injection Solution 50 mL Recalled by Cantrell Drug Company Due to Lack of Sterility Assurance.

Date: July 14, 2017
Company: Cantrell Drug Company
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Cantrell Drug Company directly.

Affected Products

Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222

Quantity: 40081 syringes

Why Was This Recalled?

Lack of Sterility Assurance.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Cantrell Drug Company

Cantrell Drug Company has 52 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report