The U.S. Food and Drug Administration (FDA) said reports of faulty Philips ventilators and sleep apnea machines had risen in the past quarter, underlining
The US public health watchdog FDA said it had received nearly 50,000 reports against Philips in just three months. The Dutch giant has already had to recall millions of its devices.
By Toby Sterling and Bart H. Meijer AMSTERDAM (Reuters) - The U.S. Food and Drug Administration (FDA) said reports of faulty Philips ventilators and s.
By Toby Sterling and Bart H. Meijer AMSTERDAM (Reuters) - The U.S. Food and Drug Administration (FDA) said reports of faulty Philips ventilators and s.
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