[Recalled] NIDEK Medical NUVO LITE MODEL 925 OCSI, 230V - 50Hz - 300W. Oxygen Concentrator. — Capacitor failure may result in a fire hazard and loss of supplemental oxygen | FDA 2012-05-01
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | NIDEK Medical NUVO LITE MODEL 925 OCSI, 230V - 50Hz - 300W. Oxygen Concentrator. |
|---|---|
| Brand / manufacturer | Nidek Medical Products Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1780-2012 |
| 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.
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