Official recall record

Transfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamp)

Health Canada — Medical Devices · 2024-10-31 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2024-10-31
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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