Philips Voluntary 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 …

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

https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-classifies-recall-philips-respiratory-devices-most-serious-2023-02-16/

2 days ago · Follow. Feb 16 (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' (PHG.AS) …

Active Philips Respironics Field Service Actions

https://www.usa.philips.com/healthcare/e/sleep/communications/active-field-service-actions

Initiated August 2022. Philips’ subsidiary Philips Respironics has expanded its voluntary April 2021 recall notification/field safety notice for 43 A-series BiPAP ventilators (A30, …

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 Respironics CPAP, BiPAP, and Ventilator Recall: …

https://www.fda.gov/medical-devices/safety-communications/faqs-philips-respironics-ventilator-bipap-machine-and-cpap-machine-recalls

Philips Respironics (Philips) voluntarily recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and …

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 …

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

Reason for Recall. Philips is recalling certain reworked Philips Trilogy 100, Trilogy 200, ... Phillips sent affected customers an Urgent Medical Device Recall letter in …

URGENT: Medical Device Recall - Philips

https://www.philips.com/c-dam/b2bhc/master/landing-pages/src/update/documents/philips-recall-letter-2021-05-a-2021-06-a.pdf

Philips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips …

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 · February 16, 2023, 6:12 PM · 1 min read. Feb 16 (Reuters) - U.S. health regulators on Thursday classified the recall of Dutch medical device maker Philips' …

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