ProductGuru Recalls

Official recall record

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

US FDA — Medical Devices · 2024-10-21 · United StatesClass I
Issuing authority
US FDA — Medical Devices
Alert date
2024-10-21
Country of alert
United States
Alert level
Class I
Alert type
recall
Barcode (EAN/GTIN)
00085412476261
Brand on record
Baxter Healthcare Corporation

What the authority reported

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.

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: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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Other recalls from this brand

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