Class II — Baxter Healthcare Corp.
| Recalling firm | BAXTER HEALTHCARE CORPORATION |
|---|---|
| Registered facility | View this company's 32 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger. |
| Product | Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis. |
| Quantity | 55 units |
| Distribution | Nationwide Distribution including GA, MA, NC, NY, PA, and WA. |
| Initiated | 2014-04-24 |
| Classified | 2015-01-07 |
| Terminated | 2017-07-21 |
| Recall number | Z-0932-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Baxter Healthcare Corp. (Z-0932-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69586/
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