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Home » FDA TO MEET WITH RESPIRONICS OVER TORN VENTILATOR VALVES
FDA TO MEET WITH RESPIRONICS OVER TORN VENTILATOR VALVES
February 13, 2004
The FDA is calling for a regulatory meeting with Respironics to determine why the Carlsbad, Calif.-based manufacturer repeatedly failed to submit medical device reports (MDRs) in connection with defective check valves on its Espirit ventilator.