Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution — Class II medical device recall Z-1213-2023
Ongoing recall by Baxter Healthcare Corporation, reported 2023-03-15, distributed nationwide. MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches, which may have been incorrectly seal
| Recall number | Z-1213-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2023-02-01 |
| Classified | 2023-03-03 |
| Reported by FDA | 2023-03-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 33,866,400 units |
| UPC / GTIN / UDI-DI | 00085412007694 |
| Lot numbers | GD912051, GD912068, GD912099, GD912112, GD912143, GD912204 |
| Expiration dates | 2024-03-31, 2024-04-30, 2024-05-31 |
Product
Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for peritoneal dialysis
Reason for recall
MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. This could lead to exposure to air, resulting in insufficient iodine/dry sponge inside the MiniCap, which could lead to the potential for inadequate disinfectant.
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-1213-2023. 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.