Class II — Invacare Corporation
| Recalling firm | Invacare Corporation dba Invacare America |
|---|---|
| Registered facility | View this company's 7 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The firm has found that the Component- Dianz Capacitor has ruptured which results in a potential fire hazard. |
| Product | Component- Dianz Capacitor used in PerfectO2 Oxygen Concentrator, packaged one unit per box. |
| Quantity | 138,446 units distributed globally |
| Distribution | The product was distributed throughout the U.S. and to foreign countries, including Canada and other countries TBD. The affected product was also distributed to eight government consignees. |
| Initiated | 2014-10-31 |
| Classified | 2014-12-24 |
| Terminated | 2017-02-07 |
| Recall number | Z-0872-2015 |
| 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 — Invacare Corporation (Z-0872-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69873/
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