A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Respironics, Inc., Trilogy 100, 200, and 202 Ventilators: Class I Recall – Power Supply May Fail. According to the Food & Drug Administration FDA’s MedWatch:
Ventilator power supply failure may lead to unexpected cessation of ventilation and failure of alarm to sound.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Respironics, Inc., Trilogy 100, 200, and 202 Ventilators: Class I Recall – Power Supply May Fail.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
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