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Baxter Healthcare Corporation recalls Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
Recalled September 21, 2022 · FDA recall Z-1653-2022 · Baxter Healthcare
Hazard
Firm noted an increase in customer reports of leaks. · FDA Class I
Units
511,728 units
Sold at
US Nationwide Distribution
Description
Firm noted an increase in customer reports of leaks.
Product
Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →