The U.S. Food and Drug Administration (FDA) on Tuesday classified the recent recall of some of Philips’ ventilators as Class 1, or the most serious type of recall, saying the use of these devices may cause serious injuries or death. This is the second Class 1 recall initiated by the company this year. In June,…
FDA Classifies Philips Ventilator Recall Due to Low Oxygen Risk
The U.S. Food and Drug Administration (FDA) on Tuesday classified the recent recall of some of Philips’ ventilators as Class 1, or the most serious type of recall, saying the use of these devices may cause serious injuries or death. This is the second Class 1 recall initiated by the company this year. In June,…
FDA Classifies Philips Ventilator Recall as Most Serious
The Food and Drug Administration (FDA) on Thursday classified the recall of Philips’ breathing devices and ventilators as Class 1, or the most serious type of recall, saying the use of these devices may cause serious injuries or death. The agency said there have been 83 complaints regarding the products used to provide breathing assistance,…
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