Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp — Class I medical device recall Z-0377-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2024-11-27, distributed nationwide. Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dio
| Recall number | Z-0377-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-10-21 |
| Classified | 2024-11-20 |
| Reported by FDA | 2024-11-27 |
| Distributed | Nationwide (US) |
| Quantity | 410,862 units |
| UPC / GTIN / UDI-DI | 00085412007748 |
| Model numbers | R5C4482 |
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0377-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.