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Philips Respironics Recall Page: https://www.usa.philips.com/healthcar... FDA Recall Update https://www.fda.gov/news-events/press... On November 12 the FDA released an update related to the June 14 Philips Respironics Recall announcement. The FDA has conducted an inspection of one of Philips Respironic's manufacturing facilities. The FDA investigator provided a list of their observations to the company. From my interpretation, Philips did know about the degradation of the foam in the Trilogy ventilators. They had even started a corrective and preventive action plan that was not formally submitted. Records of the plan, date back to April 12, 2018. They were already doing preventive maintenance on the Trilogy ventilators prior to the June 14 Recall announcement. Chapters: 00:00 Intro 00:25 FDA Inspection of Philips Respironics foam 01:29 Philips Respironics' plan 02:50 What does this all mean? 03:27 Consequences of a potentially defective replacement foam 04:04 Where Sleeplay stands 05:09 Coming together during hard times Shop Online: Our Store: https://sleeplay.com CPAP Machines: https://sleeplay.com/collections/cpap... CPAP Masks: https://sleeplay.com/collections/cpap... CPAP Cleaning: https://sleeplay.com/collections/cpap... CPAP Supplies: https://sleeplay.com/collections/cpap... Oxygen Therapy: https://sleeplay.com/collections/oxyg... Go Social: Facebook: / sleeplayground Instagram: / sleeplayground Twitter: / sleeplayground TikTok: / sleeplayground