MiniCap Extended Life PD Transfer Set — Class II medical device recall Z-0768-2021
Terminated recall by Baxter Healthcare Corporation, reported 2021-01-13, distributed nationwide. Potential for no-flow and leaks under the twist clamp.
| Recall number | Z-0768-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2020-11-10 |
| Classified | 2021-01-04 |
| Reported by FDA | 2021-01-13 |
| Terminated | 2023-03-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | BM, BR, CA, ID, MX |
| Quantity | 72,771 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00085412007731 |
| Lot numbers | H20D13100, H20D27084, H20D30070, H20E13107, H20E19054, H20E22082, H20F09061, H20F15050, H20F18070, H20F24086, H20F29051, H20G13046, H20G27087, H20G30065, H20H05057, H20H14067, H20H19066 |
Product
MiniCap Extended Life PD Transfer Set
Reason for recall
Potential for no-flow and leaks under the twist clamp.
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-0768-2021. 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.