Philips Medical Device Recall

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Medical Device Recall Information - Philips Respironics …

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only). We …

Philips Recall: 82 More Death Reports in Medical Device Reports

https://sleepreviewmag.com/sleep-treatments/therapy-devices/cpap-pap-devices/philips-recall-82-more-death-reports-medical-device-reports/

The latest data update from Nov 1 to Dec 31 adds 82 more reports of deaths to the medical device reports. Since April 2021, the FDA has received more than 98,000 …

Philips Respironics Recalls Certain Reworked Philips …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-reworked-philips-respironics-trilogy-100200-and-garbin

Philips Respironics Recalls Certain Reworked Philips Respironics Trilogy 100/200 and Garbin Ventilators Due to Potential for Silicone Foam Adhesion Failure and …

How Philips’ significant respiratory devices recall unfolded

https://www.massdevice.com/how-philips-significant-respiratory-devices-recall-unfolded/

Philips’ first recall notification involved specific Philips bi-level positive airway pressure (bi-level PAP), continuous positive airway pressure (CPAP) and mechanical ventilator …

URGENT Medical Device Recall - usa.philips.com

https://www.usa.philips.com/c-dam/b2bhc/master/landing-pages/src/update/documents/en_US/trilogy/trilogy-field-safety-notice-en-us.pdf

URGENT Medical Device Recall Trilogy 100 and Trilogy 200 Silicone Sound Abatement Foam Delamination Dear Customer, Philips Respironics has detected an issue impacting …

Philips CPAP Recall: Related MDRs Top 98K, Including 346 Deaths

https://www.drugwatch.com/news/2023/02/16/philips-cpap-recall-deaths/

Philips CPAP Recall Status Following the initial recall of Philips CPAP, BIPAP and ventilator machines in June 2021, predominantly from the DreamStation line …

Philips recalls certain reworked Trilogy, Garbin ventilators

https://www.massdevice.com/philips-recalls-reworked-trilogy-garbin-ventilators/

1 day ago · The FDA notice includes devices distributed between March 1, 2022, and Sept. 6, 2022. Devices recalled in the U.S. total 13,811 since Philips initiated the recall on …

U.S. FDA classifies recall of Philips' respiratory devices as most …

https://finance.yahoo.com/news/u-fda-classifies-recall-philips-231246716.html

2 days ago · Feb 16 (Reuters) - U.S. health regulators on Thursday classified the recall of Dutch medical device maker Philips' respiratory machines as most serious, saying their …

U.S. FDA classifies recall of Philips' respiratory devices as most ...

https://health.economictimes.indiatimes.com/news/medical-devices/u-s-fda-classifies-recall-of-philips-respiratory-devices-as-most-serious/98014435

2 days ago · Its subsidiary, Philips Respironics, had in December also recalled about 13,811 ventilators which were distributed between March 1, 2022 and Sept. 6, 2022. There were …

Medical Device Recall Information - philips.ca

https://www.philips.ca/healthcare/e/sleep/communications/src-update/news/update-on-completed-set-of-test-results-for-first-generation-dreamstation

We know that patients depend on Philips Respironics devices for their health and well-being. We deeply regret that for many patients, the voluntary recall …

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