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Medical Device Recall Information - Philips Respironics …
- 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 …
Medical Device Field Safety Notice (Outside of U.S.)
- https://www.philips.com/c-w/corporate-homepage/src-update/information-for-physicians-and-providers.html
- Philips Respironics announced a voluntary recall notification (U.S. only) / field safety notice (Outside of U.S.) for Continuous and Non-Continuous Ventilators (certain CPAP, …
Certain Philips Respironics Ventilators, BiPAP, and …
- https://www.fda.gov/medical-devices/safety-communications/certain-philips-respironics-ventilators-bipap-and-cpap-machines-recalled-due-potential-health-risks
Active Philips Respironics Field Service Actions
- https://www.usa.philips.com/healthcare/e/sleep/communications/active-field-service-actions
- Voluntary field safety notice of V60 ventilator product family Initiated October 2022 There is a possibility that affected ventilator units may cease to operate, potentially without setting …
Sleep respiratory recall | Philips
- https://www.philips.com.sg/healthcare/e/sleep/communications/src-update
- 1800-28-63-020 In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary …
AED Pads Medical Device Correction Notice | Philips
- https://www.usa.philips.com/healthcare/resources/landing/pads-medical-device-correction
- Important information for the continued safe and proper use of your equipment. Urgent Medical Device Correction (1.16MB) 1-800-263-3342. Philips is notifying customers of a …
Sleep and respiratory care update | Philips
- https://www.philips.com/c-w/corporate-homepage/src-update.html
- Philips Respironics. There is nothing we take more seriously than providing patients with high quality products that are safe and reliable. If an issue arises, we are proactive in …
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 Dec. …
FDA: Nearly 350 Deaths Linked to Recalled Philips CPAP Machines
- https://www.consumernotice.org/news/nearly-350-deaths-linked-to-recalled-philips-cpap-machines/
- “The vast majority (93%) of the approximately 99,000 MDRs filed since April 2021 up to and including December 2022 are alleged technical malfunctions that do not …
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