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[Recalled] NIDEK Medical M5C5/ MARK5 NUVO/OCSI, 230 V~50/60 Hz -420 W. Oxygen Concentrator. — Capacitor failure may result in a fire hazard and loss of supplemental oxygen | FDA 2012-05-01

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductNIDEK Medical M5C5/ MARK5 NUVO/OCSI, 230 V~50/60 Hz -420 W. Oxygen Concentrator.
Brand / manufacturerNidek Medical Products Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1775-2012
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date01 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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