LVP Blood Products Administration Set Dual-Inlet — Class II medical device recall Z-2233-2025
Ongoing recall by Fresenius Kabi USA, LLC, reported 2025-08-06, distributed nationwide. Potential for external cassette leaks
| Recall number | Z-2233-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Kabi USA, LLC, North Andover, MA, United States |
| Recall initiated | 2025-06-24 |
| Classified | 2025-07-31 |
| Reported by FDA | 2025-08-06 |
| Distributed | Nationwide (US) |
| Quantity | 14,280 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00811505030030 |
| Lot numbers | FA24K05023, FA24L02010, FA24L04198, FA24L04214 |
Product
LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
Reason for recall
Potential for external cassette leaks
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-2233-2025. 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.