Baxter Healthcare Corporation (Baxter) is issuing an urgent medical device correction for the Minicap Extended Life Pd Transfer Sets listed, which are manufactured with peroxide-cured silicone tubing that transfers solution to and from the patient. Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to nondioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices. The source of the NDL PCBAs and/or NDL PCBs in those recalls was due to the manufacturing process of the silicone tubing. Recall Start Date: October 21, 2024
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