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Baxter Healthcare Corporation recalls Effluent Sample Bag
Recalled June 8, 2022 · FDA recall Z-1144-2022 · 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
78 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
Effluent Sample Bag
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →