Key Takeaways The US Food and Drug Administration (FDA) is monitoring a voluntary, firm-initiated Class II recall of DELFLEX peritoneal dialysis solutions (1.5% and 2.5% dextrose, 2L 5-pack), involving over 80 000 bags distributed nationwide and identified across multiple lots including 25CU02007–25CU02009 and 25CU02002, 25CU02011–25CU02013. The recall was initiated by Fresenius Medical Care Holdings, Inc.