FDA Device recall Z-2597-2018
power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320 by Baxter Healthcare, citing there were instances where the power cord socket detached from the back of the AMIA cycler when the power cord was unplugged from the socket.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2597-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-12 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320; (b) Kaguya PD System, Product Code: T5C8500 (Japanese distribution only)
Reason
There were instances where the power cord socket detached from the back of the AMIA cycler when the power cord was unplugged from the socket.
Identifiers
| code_info | All Serial Numbers |
|---|
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-2597-2018%22
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