Philips North America Llc 2025-05-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1722-2025
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub… Recall
Issued May 14, 2025 · Philips North America Llc
In May 2025, Philips North America Llc recalled the Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
What you should do
- 1 Stop using Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America Llc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Philips North America Llc
- Category
- Health
- Recall date
- May 14, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of AE, AL, AO, AR, AT, AU, AW, BD, BE, BG, BH, BO, BR, BW, BY, CA, CD, CH, CI, CL,
- Recall number
- FDA-Z-1722-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America Llc has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.