Reported May 14, 2025 · Ongoing
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi…
Philips North America LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity , Adt/Pedi Intub CO2 Line LTerm Lng , Adt/Pedi Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line LTerm , Neo/Inf Intub CO2 Line High Humidity , Neo/Inf Intub CO2 Line LTerm Lng , VitaLine H Set Adult/Pediatric , VitaLine H Set Infant/Neonatal , FilterLine Set Long Adult/Pediatric , FilterLine H Set Long Adult/Pediatric , FilterLine H Set Long Infant/Neonatal
- Trade CompliantFilterLine H, Adult/Ped
- Trade CompliantFilterLine H, Infant/Neo , FilterLine Set Adult/Pedi , FilterLine H Set Adult/Pedi and FilterLine H Set Infant/Neonatal. Carbon dioxide gas analyzer
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 989803204511989803204321989803204301989803204331989803204521989803204531989803204311989803204341989803159571989803159581989803160241989803160251989803160261989803182921989803182931989803105531989803105541989803105561989803204321, 989803204301, 989803204331, 989803204521, 989803204531, 989803204311, 989803204341, 989803159571, 989803159581, 989803160241, 989803160251, 989803160261, 989803182921, 989803182931, 989803105531, 989803105541, 989803105561 — UDI: N/A — 989803105531989803105541989803105561989803159581989803160241989803160251989803160261989803182921989803182931989803204301989803204311989803204321989803204331989803204341989803204511989803204521989803204531989803159571989803159581989803160241989803160251989803160261989803182921989803182931989803204301989803204311989803204321989803204331989803204341989803204511989803204521989803204531System Codes 989803105531, 989803105541, 989803105561, 989803159581, 989803160241, 989803160251, 989803160261, 989803182921, 989803182931, 989803204301, 989803204311, 989803204321, 989803204331, 989803204341, 989803204511, 989803204521, 989803204531, 989803159571, 989803159581, 989803160241, 989803160251, 989803160261, 989803182921, 989803182931, 989803204301, 989803204311, 989803204321, 989803204331, 989803204341, 989803204511, 989803204521, 989803204531, M1920A, M1921A, M1923A. - Amount recalled
- 486,631 units
Where it was sold
Why it was recalled
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
This product could cause temporary or reversible health problems — stop using it.
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