Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp — Class II medical device recall Z-2246-2017
Terminated recall by Baxter Healthcare Corporation, reported 2017-06-14, distributed nationwide. Connection issues between the PD transfer set catheter connector and an adapter may lead to leaks and contamin
| Recall number | Z-2246-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2014-04-28 |
| Classified | 2017-06-02 |
| Reported by FDA | 2017-06-14 |
| Terminated | 2017-07-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MY |
| Quantity | 6,048 |
| Reason classes | packaging |
| Lot numbers | H12030047 |
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit. Sterile. Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Reason for recall
Connection issues between the PD transfer set catheter connector and an adapter may lead to leaks and contamination of the fluid pathway which may result in peritonitis.
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-2246-2017. 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.