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Baxter Healthcare Corporation recalls 3,65 m Extension Set with Luer-lock Connector
Recalled June 8, 2022 · FDA recall Z-1145-2022 · Baxter Healthcare
Hazard
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error. · FDA Class II
Units
60 units
Sold at
US Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.
Description
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Product
3,65 m Extension Set with Luer-lock Connector
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →