Baxter Amia Automated PD systems are used in the treatment of adult… — Class II medical device recall Z-0932-2015
Terminated recall by Baxter Healthcare Corp., reported 2015-01-14, distributed nationwide. System error 01779 is produced when the battery cannot be charged due to specific voltage differences between
| Recall number | Z-0932-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp., Deerfield, IL, United States |
| Recall initiated | 2014-04-24 |
| Classified | 2015-01-07 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2017-07-21 |
| Distributed | Nationwide (US) |
| Quantity | 55 units |
Product
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.
Reason for recall
System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.
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-0932-2015. 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.