Baxter Healthcare Corporation recalls Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Singl
Recalled September 11, 2024 · FDA recall D-0649-2024 · Baxter Healthcare
Hazard
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing. · FDA Class I
Units
44,208 containers
Sold at
Nationwide in the USA
Description
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Product
Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Baxter USA, NDC 0338-0433-04
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →