Trilogy Ventilator Models 100, 200 and 202 by Philips Respironics: Recall
MedSun: Newsletter #93, March 2014

FDA MedWatch Safety Alert

Ventilators due to a potentially defective component on the Trilogy Ventilator power management board, which could affect the function of the device. If this issue is not corrected it is possible that the ventilator may fail to deliver mechanical breaths and that the alarm functionality may be reduced to indicate ventilatory failure. Customers should remove affected devices from service and to return them to Philips for replacement. All distributors, providers, and customers with potentially affected Trilogy devices will have their units replaced.

Additional Information:

Trilogy Ventilator Models 100, 200 and 202 by Philips Respironics: Recall. FDA MedWatch Safety Alert. February 20, 2014.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm386561.htm


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