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The FDA is clarifying language related to the direct marking of medical devices for unique device identification purposes, including the definition of reprocessing. Read More
Philips is advising clinicians not to use its adaptive servo-ventilation therapy devices to treat sleep apnea and chronic heart failure in light of recent safety risks that were revealed in a Phase 3 study. Read More
BD’s CareFusion subsidiary issued an update on its recall of the Avea ventilator to provide clarification on certain units of the product. The device is intended for continuous breathing support in infants through adults. Read More