Cantrell Drug Company recalls Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company
Recalled August 16, 2017 · FDA recall D-1075-2017 · Cantrell Drug
Hazard
Lack of Sterility Assurance. · FDA Class II
Units
40081 syringes
Sold at
Nationwide within the US
Description
Lack of Sterility Assurance.
Product
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
Manufacturer(s)
Cantrell Drug Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →