PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 16, 2017 Initiated: July 14, 2017 #D-1075-2017

Product Description

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

Reason for Recall

Lack of Sterility Assurance.

Details

Recalling Firm
Cantrell Drug Company
Units Affected
40081 syringes
Distribution
Nationwide within the US
Location
Little Rock, AR

Frequently Asked Questions

What product was recalled?
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. Recalled by Cantrell Drug Company. Units affected: 40081 syringes.
Why was this product recalled?
Lack of Sterility Assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 16, 2017. Severity: Moderate. Recall number: D-1075-2017.