Philips recalls neonatal and infant intubation CO2 filter lines due to potential difficulty disconnecting adapters from endotracheal tubes. Affected models include specific part numbers and system codes.
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
Philips is recalling certain neonatal and infant intubation CO2 filter lines because the adapter may disconnect from the endotracheal tube, which could cause breathing issues. This recall affects healthcare providers using these devices in hospitals or clinics.
The adapter on the CO2 filter line can become difficult or impossible to disconnect from the endotracheal tube. This could lead to breathing problems for infants or neonates during medical procedures if the connection is not properly maintained.
Healthcare providers using the recalled CO2 filter lines in neonatal and infant care settings are most at risk. These devices are typically used in hospitals and clinics for breathing support in newborns and infants.
Check for model numbers 989803204511, 989803204321, and other listed part numbers. The product is marketed as Adt/Pedi Intub CO2 Line STerm, Adt/Pedi Intub CO2 Line LTerm, or similar names. These items were sold in hospitals and clinics for neonatal and infant care.
Look for model numbers on the device, such as 989803204511 or 989803204321.
Reach out to Philips customer service for assistance with the recall and possible remedies.
The recall includes specific model numbers like 989803204511, 989803204321, and other listed part numbers. The product is marketed as Adt/Pedi Intub CO2 Line STerm, Adt/Pedi Intub CO2 Line LTerm, and similar names.
The adapter on the CO2 filter line can become difficult or impossible to disconnect from the endotracheal tube, which could cause breathing issues for infants or neonates.
No, but healthcare providers should check if they have the affected models and contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1722-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1722-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
