Cantrell Drug Company recalls Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use On
Recalled December 21, 2016 · FDA recall D-0192-2017 · Cantrell Drug
Hazard
Lack of Assurance of Sterility - the firm is recalling select sterile drug products. · FDA Class II
Units
1494 syringes
Sold at
Nationwide
Description
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Product
Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16
Manufacturer(s)
Cantrell Drug Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →