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Philips Respironics CPAP, BiPAP recall is Class I

The FDA today issued a notice confirming that a recall of Philips Respironics face masks is Class I, the most serious kind.

Roy jakobsPhilips respironicsDavid fergusonUs department of justiceSamara viewWisp youthTherapy maskConnected care

Philips recalls 17M CPAP, BiPAP masks over magnets that could affect implanted devices

The mask recall was announced after 14 serious injuries were reported, including pacemaker failure, arrhythmia, seizures, and irregular blood pressure, the FDA said.

United statesJeff shurenPhilips respironicsRadiological healthDrug administrationSamara viewWisp youthWisp youth nasal maskTherapy maskMagnetic resonanceHealth care

Philips Respironics Recalling More Than 17 Million CPAP, BiPAP Masks

Magnets in the recalled masks, used in breathing machines for sleep apnea, can interfere with pacemakers and other lifesaving medical devices.

Jeff shurenPhilips respironicsPhilips respironicRadiological healthDrug administrationSamara viewWisp youth

Philips recalls 17M CPAP, BiPAP masks over magnets that could affect implanted devices

The mask recall was announced after 14 serious injuries were reported, including pacemaker failure, arrhythmia, seizures, and irregular blood pressure, the FDA said.

United statesJeff shurenPhilips respironicsRadiological healthDrug administrationSamara viewWisp youthWisp youth nasal maskTherapy maskMagnetic resonanceHealth care

Philips recalls 17M CPAP, BiPAP masks over magnets that could affect implanted devices

The mask recall was announced after 14 serious injuries were reported, including pacemaker failure, arrhythmia, seizures, and irregular blood pressure, the FDA said.

United statesJeff shurenPhilips respironicsRadiological healthDrug administrationSamara viewWisp youthWisp youth nasal maskTherapy maskMagnetic resonanceHealth care

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