FDA Philips Respironics Updates Use Instructions For Bipap A30, A40, And V30 Devices
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Koninklijke Philips NV 
PHIA:
FDA: PHILIPS RESPIRONICS UPDATES USE INSTRUCTIONS FOR BIPAP A30, A40, AND V30 DEVICES DUE TO INTERRUPTIONS AND/OR LOSS OF THERAPY
FDA: PHILIPS RESPIRONICS' RECALL FOR CORRECTING DEVICES & NOT REMOVING FROM WHERE THEY ARE USED OR SOLD; FDA CLASSIFIES RECALL AS MOST SERIOUS TYPE
FDA: HAVE BEEN 13 REPORTED INJURIES. AND EIGHT REPORTS OF DEATH FROM PHILIPS RESPIRONICS BIPAP A30, A40, AND V30 DEVICES
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