Class II — Oxus America, Inc.
| Recalling firm | Oxus America Inc |
|---|---|
| Registered facility | Oxus America, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Due to past battery inventory storage conditions and deficiencies in the maintenance procedure, it was possible that some batteries were over-discharged to point of damaging the cells. |
| Product | Li-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400. Also branded as Reliability Plus byDrive. The Portable Oxygen Concentrator is intended to deliver concentrated oxygen for adult patients with chronic pulmonary diseases. |
| Quantity | 1724 total units |
| Distribution | Worldwide Distribution-USA including the states of New York, Michigan, Colorado, Texas, Iowa, Florida, Georgia, Ohio, Wisconsin, Oregon, Alabama, Illinois, Utah, Oklahoma, West Virginia and California and the countries of Canada, European Union, South Africa, Korea and Brazil. |
| Initiated | 2013-01-14 |
| Classified | 2013-02-02 |
| Terminated | 2013-07-17 |
| Recall number | Z-0768-2013 |
| 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 — Oxus America, Inc. (Z-0768-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64057/
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