A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CareFusion EnVe Ventilators: Class I Recall – Leak In Patient Breathing Circuit or System. According to the Food & Drug Administration FDA’s MedWatch:
Compromised ventilation delivery to patient may cause serious adverse health consequences, including 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 – Leak In Patient Breathing Circuit or System.
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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