House, nursing home fires spur Nidek oxygen concentrator recall
Alabama-based oxygen devices maker Nidek Medical pulled its Mark5 Nuvo oxygen concentrators off of shelves after receiving reports of fires in homes and nursing homes, according to an FDA release.
The company pulled 8 Mark 5 models after finding that a capacitor component in some devices failed and "resulted in residential and North GA Nursing Degree as well as failing to provide oxygen.
The recall has been given "Class I" status from the FDA, reserved for the highest risk recalls that are likely to result in patient injury or death.
The oxygen concentrator devices are not considered life-supporting, and no injuries have been reported to date, according to the release.
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MicroMed wins IDE approval to launch a clinical trial of its HeartAssist 5
Houston, Texas-based MicroMed Cardiovascular won FDA investigational device exemption to launch human trials of its next-generation HeartAssist 5 left-ventricular assist device in up to 192 patients.
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Bausch & Lomb wins FDA approval for enVista intraocular lens
California-based eye care giant Bausch & Lomb won FDA pre-market approval for its enVista hydrophobic intraocular lens, which it calls "the 1st and only FDA-approved IOL in the U.S. with labeling that states: ‘No glistenings of any grade were reported for any subject at any visit in the clinical study’."
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