Baxter MiniCap Extended Life PD Transfer Set — Class II medical device recall Z-0569-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2024-12-04. There has been an increase in the number of complaints related to the separation of the female connector from
| Recall number | Z-0569-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-10-23 |
| Classified | 2024-11-27 |
| Reported by FDA | 2024-12-04 |
| Quantity | 13,376 units |
| UPC / GTIN / UDI-DI | 00085412150703 |
| Serial numbers | H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062 |
| Model numbers | T5C4326K |
Product
Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis
Reason for recall
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
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-0569-2025. 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.