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Megadyne Reiterates Intended Use Population Change for Megadyne Mega Soft Universal and Universal Plus Patient Return Electrodes - Vimarsana News

Megadyne Reiterates Intended Use Population Change for Megadyne Mega Soft Universal and Universal Plus Patient Return Electrodes

Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA S

Source: fda.gov
Philips North America LLC Recalls Panorama 1.0T HFO Due to a Risk of Explosion - Vimarsana News

Philips North America LLC Recalls Panorama 1.0T HFO Due to a Risk of Explosion

The FDA has identified this as a Class I recall, the most serious type of recall