FDA Device recall Z-2246-2017
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit
- FDA Device
- Class II
- terminated
- Published 2017-06-14
On 2017-06-14 the FDA classified a Class II recall of Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit by Baxter Healthcare, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2246-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-28 |
| Published | 2017-06-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit. Sterile. Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Reason
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.
Identifiers
| code_info | Product Code 5C4483; Lot# H12030047 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2246-2017%22
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