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www.fdanews.com/articles/147389-oxygen-devices-recalled

Oxygen Devices Recalled

June 21, 2012
The FDA has issued a class I recall for several models of oxygen concentrators because of a potential fire hazard. A capacitor failure in the Nidek Medical Mark5 Nuvo and Nuvo Lite may cause fire and loss of supplemental oxygen, according to a statement from manufacturer.
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