Baxter MiniCap with Povidone-Iodine Solution — Class II medical device recall Z-2074-2014
Terminated recall by Baxter Healthcare Corp., reported 2014-07-23, distributed nationwide. Inadequate iodine and packaging related defects.
| Recall number | Z-2074-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp., Deerfield, IL, United States |
| Recall initiated | 2014-06-17 |
| Classified | 2014-07-17 |
| Reported by FDA | 2014-07-23 |
| Terminated | 2015-04-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 585,360 units |
Product
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Reason for recall
Inadequate iodine and packaging related defects.
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-2074-2014. 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.