A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Oridion Medical and Philips Healthcare Microstream CO2 Filterline (FilterLine H Set Infant/Neonate, VitaLine H Set Infant/Neonate: Recall – Plastic Strands on the Adapter May Become Dislodged, Inhaled by Patient. According to the Food & Drug Administration FDA’s MedWatch:
Inhalation of the plastic strands may cause respiratory compromise, which could result in serious illness 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: Oridion Medical and Philips Healthcare Microstream CO2 Filterline (FilterLine H Set Infant/Neonate, VitaLine H Set Infant/Neonate: Recall – Plastic Strands on the Adapter May Become Dislodged, Inhaled by Patient.
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.