MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S — Class II medical device recall Z-0831-2022
Terminated recall by Baxter Healthcare Corporation, reported 2022-04-06, distributed nationwide. Devices distributed lacked regulatory clearance.
| Recall number | Z-0831-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-02-25 |
| Classified | 2022-03-29 |
| Reported by FDA | 2022-04-06 |
| Terminated | 2026-05-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | MX |
| Quantity | 498 units |
| UPC / GTIN / UDI-DI | 00085412008776, 00085412008783, 00085412050768, 00085412476261 |
| Lot numbers | H17H03057, H18A12037, H18E18050, H18G16076, H19E31052, H20F02074, H20K06035, H20K06084, H20L08070, H21B16056, H21C31053, H21E07058, H21F07049, H21F08070, H21F28060, H21K16066 |
Product
MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S, R5C4482, R5C4483, R5C4484
Reason for recall
Devices distributed lacked regulatory clearance.
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-0831-2022. 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.