[Recalled] NIDEK Medical NUVO LITE MODEL 925 OCSI, 3LPM 230V - 60Hz - 280W. Oxygen Concentrator. — Capacitor failure may result in a fire hazard and loss of supplemental oxygen | FDA 2012-05-01
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | NIDEK Medical NUVO LITE MODEL 925 OCSI, 3LPM 230V - 60Hz - 280W. Oxygen Concentrator. |
|---|---|
| Brand / manufacturer | Nidek Medical Products Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1781-2012 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 01 May 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Nidek Medical Products Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.