FDA Device recall Z-0932-2015
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis
- FDA Device
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis by Baxter Healthcare, citing system error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0932-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-24 |
| Published | 2015-01-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.
Reason
System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.
Identifiers
| code_info | Product Code: 5C9310 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0932-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.