Philips Respironics alerts customers worldwide of updated instructions and labeling of specific sleep therapy masks that contain magnetic headgear clips due to potential risk of serious injury
September 06, 2022 16:00 ET | Royal Philips
September 6, 2022 These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical...
Philips provides update on Philips Respironics’ PE-PUR sound abatement foam test and research program
June 28, 2022 01:55 ET | Royal Philips
June 28, 2022 Testing in accordance with ISO 18562 and ISO 10993 standards conducted by five certified, independent testing laboratories in the US and Europe Amsterdam, the...
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Philips Respironics issues voluntary recall notification/field safety notice* for the V60 ventilator product family
April 22, 2022 11:00 ET | Royal Philips
April 22, 2022 Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that its subsidiary Philips Respironics is notifying customers...
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Philips Respironics provides update for the US on ongoing CPAP, BiPAP and Mechanical Ventilator field action
March 10, 2022 19:15 ET | Royal Philips
March 10, 2022 Amsterdam, the Netherlands – Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, today provided an update on the remediation status in the US of the ongoing...
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Philips provides update on the test and research program in connection with the CPAP, BiPAP and Mechanical Ventilator recall notification*
December 23, 2021 02:00 ET | Royal Philips
December 23, 2021 Amsterdam, the Netherlands – On June 14, 2021, Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, initiated a voluntary recall notification* for certain sleep...
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Philips provides update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification*
November 14, 2021 05:00 ET | Royal Philips
November 14, 2021 Amsterdam, the Netherlands – On June 14, 2021, Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, initiated a voluntary recall notification* for certain...
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Philips starts repair and replacement program of first-generation DreamStation devices in the US in relation to earlier announced recall notification*
September 01, 2021 02:00 ET | Royal Philips
September 1, 2021 Amsterdam, the Netherlands – Royal Philips (NYSE: PHG; AEX: PHIA) today announced an update in connection with the June 14, 2021 recall notification* for specific Philips sleep and...
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Philips issues recall notification* to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices
June 14, 2021 01:00 ET | Royal Philips
June 14, 2021 Philips is initiating a voluntary recall notification* to ensure patient safety in consultation with regulatory agenciesCorrective actions include the deployment of updated instructions...
Philips survey reveals COVID-19’s negative impact on sleep quality and CPAP use
March 10, 2021 04:00 ET | Royal Philips
March 10, 2021 70% of people surveyed have experienced one or more new sleep challenges since the start of the pandemic72% of surveyed sleep apnea patients who discontinued CPAP therapy cited...
Philips details plans to increase its hospital ventilator production to 4,000 units/week by Q3 2020, and introduces its new Philips Respironics E30 ventilator with an immediate production of 15,000 units/week
April 14, 2020 08:00 ET | Royal Philips
April 14, 2020 Philips engages manufacturing partners Flex Ltd. (NASDAQ: FLEX) and Jabil (NYSE: JBL), as well as other partners, to further expand its hospital ventilator assembly lines and...