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As a result of extensive ongoing analysis following this announcement, on June 14, 2021, the company issued a recall notification (U.S. only) / field safety notice (Outside of U.S.) for specific affected devices.
===June 23, 2021 - Health Canada posted a recall for the same products.===
https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75887r-eng.php<br />
https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75889r-eng.php<br />
===June 30, 2021 - FDA Safety Communication===
Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication<br />
https://www.fda.gov/medical-devices/safety-communications/certain-philips-respironics-ventilators-bipap-and-cpap-machines-recalled-due-potential-health-risks
===July 9, 2021 - Canadian Response===
From CTV news (in Canada):
In July, the Canadian Thoracic Society, Canadian Sleep Society and the Canadian Society of Respiratory Therapists released a joint statement on the recall to help guide physicians, where they noted that “globally, the number of units affected is in the millions.”
The included link is https://cts-sct.ca/wp-content/uploads/2021/07/CTS_CSS_CSRT-Phillips-Recall-Statement_final-07_09_2021.pdf<br />
In brief, after discussion with their doctor, most patients should continue using the machine until it can be replaced with an unaffected machine, preferably sooner than later.
===July 14, 2021 - ResMed Response===
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