Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

Recall date

October 21, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0381-2025

FDA classification

Class I

Brand / firm

Baxter Healthcare Corporation

Sold / distributed

Worldwide Distribution (US Nationwide distribution)

Why it was recalled

Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis