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FDA Provides Update on Recall of Certain Philips Respironics Breathing Assistance Machines

In a news release November 12, the FDA provided an update related to the recall of certain Philips Respironics ventilators, CPAP and BiPAP machines. According to the release “during the manufacturing facility inspection, the FDA obtained additional information, not previously available to the agency, regarding the silicone-based foam used in a singular, similar device marketed outside the U.S., which failed......

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