A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CareFusion EnVe Ventilators: Class I Recall – Potential for Interruption of Patient Ventilation. According to the Food & Drug Administration FDA’s MedWatch:
Failure to adequately ventilate may lead to hypoxia or hypercarbia, which may result in serious neurological injury or death.
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: CareFusion EnVe Ventilators: Class I Recall – Potential for Interruption of Patient Ventilation.
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.
If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.