FDA classifies Philips fan recall as the most serious

July 22 (Reuters) – The U.S. Food and Drug Administration on Thursday classified the Philips Breathing Apparatus and Ventilators (PHG.AS) recall as Class 1, or the most serious type of recall, saying the recall Use of these devices can cause serious injury or death.

The agency said there had been 83 complaints about products used to provide respiratory support, but no injuries or deaths were reported for these issues.

The Dutch medical equipment company recalled some of its respirators and ventilators in June because the foam used to deaden the sound of the machines could degrade and emit small particles that irritate the airways. The gases released can also be toxic or carry cancer risks, Philips said. Read more

Report by Mrinalika Roy in Bengaluru; Editing by Devika Syamnath

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