Philips says tests on 95% of recalled devices show limited risks
Dutch medical devices maker Philips said on Tuesday (May 16) that independent tests had shown 95 per cent of its respiratory devices involved in a major global recall had shown limited health risks.
The company expects to have test results for the remaining machines involved in the recall later in the year.
Amsterdam-based Philips has been grappling with the fallout of the global recall of millions of respirators used to treat sleep apnea since it was announced in June 2021, over worries that foam used in the machines could become toxic.
It said exposure to particulate matter emissions and volatile organic compounds from degraded foam in DreamStation devices was “unlikely to result in an appreciable harm to health in patients”.
Philips had already said last year that tests indicated foam degradation was very rare and was linked to the use of unauthorised ozone-based cleaning products.
It now added that foam degradation as a result of such cleaning was also unlikely to result in an appreciable harm. Reuters
GET BT IN YOUR INBOX DAILY
Start and end each day with the latest news stories and analyses delivered straight to your inbox.
KEYWORDS IN THIS ARTICLE
BT is now on Telegram!
For daily updates on weekdays and specially selected content for the weekend. Subscribe to t.me/BizTimes
Companies & Markets
Prudential shutters Hong Kong wealth unit Pulse
Singapore has to be realistic on global trends plaguing its stock market: DPM Wong
Google DeepMind unveils next generation of drug discovery AI model
AEM Holdings Q1 net profit tumbles 85% to S$2.4 million
World’s biggest tea buyer Lipton’s sale of last farms is a strategy shift
JPMorgan, Nomura limit Segantii exposure on Hong Kong case