The FDA has announced these Class II recalls of Baxter products:
- APD Set with Cassette 3-Prong Peritoneal Dialysis Set for use with Baxter HomeChoice PD systems, because of reports of leaks. For details see http://www.accessdata.fda.gov/scripts/ires/index.cfm#Product_151903 .
- Phoenix Hemodialysis delivery system Maintenance Kit PH1, Code 6997266, lot numbers 1607250, 160824D, 161005D, and 161026D, because of incorrect component packaging. Details at http://www.accessdata.fda.gov/scripts/ires/index.cfm#Product_152438 .
- Phoenix Hemodialysis delivery system Maintenance Kit PH2, Code 6997274, lot numbers 160718E, 160720E, and 160825E, because of incorrect component packaging. Details at http://www.accessdata.fda.gov/scripts/ires/index.cfm#Product_152439 .
