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Explosion Risk Results In Class I Recall Of Philips MRI Machine

 
• By Brian Bossetta

Philips initiated a recall in November of its Panorama 1.0T magnetic resonance system due to the risk the system could explode during use. The FDA has designated the recall class I.

Philips MRI
• Source: US FDA

Philips has recalled 150 Panorama 1.0T HFO magnetic resonance (MR) systems distributed in the US between 2001 and 2016 due to the risk they could explode during a quench procedure from an excessive pressure buildup of helium gas.

During a quench — which is not common, according to the FDA —a large amount of helium evaporates and is...

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