A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Salter Labs 7600 Bubble Humidifier Used with Supplemental Oxygen Therapy: Class I Recall – Humidifier Lids Fail to Pop Off at the Intended Pressure. According to the Food & Drug Administration FDA’s MedWatch:
The humidifier can leak and can potentially interrupt the flow of supplemental oxygen to the patient.
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: Salter Labs 7600 Bubble Humidifier Used with Supplemental Oxygen Therapy: Class I Recall – Humidifier Lids Fail to Pop Off at the Intended Pressure.
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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