Philips Medical Recalls

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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 Residual PE‐PUR Foam Debris The...

Medical Device Recall Information - Philips Respironics Sleep and ...

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

This Philips Respironics December 2022 update is intended to provide healthcare providers, patients, and other stakeholders with updated information on the testing results and third party confirmed …

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 · The company's subsidiary, Philips Respironics, had recalled about 13,811 ventilators, used to provide breathing assistance to both pediatric and adult patients, …

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 …

Active Philips Respironics Field Service Actions

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

Philips’ subsidiary Philips Respironics has expanded its voluntary April 2021 recall notification/field safety notice for 43 A-series BiPAP ventilators (A30, A40, V30) …

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 issued a notice labeling the recall of certain Philips (NYSE:PHG) Respironics Trilogy and Garbin ventilators as Class I, the most serious kind This recall …

Philips Respironics Recalls Certain Continuous and Non …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-continuous-and-non-continuous-ventilators-including-cpap-and

Philips Respironics, Inc., is recalling its Continuous and Non-Continuous Ventilators due to the polyester-based polyurethane (PE-PUR) sound abatement foam, …

Philips Respironics Recalls Certain BiPAP Machines for …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-bipap-machines-plastic-issue-may-expose-patients-certain

Philips Respironics (Philips) is recalling certain BiPAP machines that may contain a plastic contaminated with a non-compatible material. If that plastic is in the …

Philips Respironics Recalls Certain Ventilators and …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-ventilators-and-bipap-machines-due-potential-health-risks-pe-pur

Philips Respironics, Inc., recalled certain ventilators and BiPAP devices due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement …

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