Cantrell Drug Company recalls Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/O
Recalled December 21, 2016 · FDA recall D-0193-2017 · Cantrell Drug
Hazard
Lack of Assurance of Sterility - the firm is recalling select sterile drug products. · FDA Class II
Units
150 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Product
Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24
Manufacturer(s)
Cantrell Drug Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →