Microstream Advance Neonatal-Infant Intubated CO2 Filter Line Neo/Inf Intub CO2 Line LTermRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 20884838093137), received between Aug 25, 2023 and Aug 25, 2023 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Suction Failure” (5 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 25, 2023Suction Failure; Suction Failure

  PHILIPS RECEIVED A COMPLAINT ON THE NEONATAL-INFANT INTUBATED CO2 FILTER LINE, EXTENDED DURATION INDICATING A POTENTIAL NEONATAL PATIENT SAFETY ISSUE DUE TO MICROSTREAM CO2 ADAPTOR & SMITHS ET TUBE STICKING TOGETHER RESULTING IN NOT BEING ABLE TO SUCTION A CRITICALLY ILL PATIENT. SOME INSTANCES RESULTED IN A PATIENT HAVING TO BE EXTUBATED SO THAT THEY CAN BE SUCTIONED AND THE AIRWAY HAVING TO BE REINSERTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17627732 ↗
• MalfunctionAug 25, 2023Suction Failure; Suction Failure

  THE CUSTOMER STATED THAT THE PATIENT REQUIRED AN ADDITIONAL MEDICAL PROCEDURE (OUTSIDE THE SCOPE OF NORMAL TREATMENT). THE REPORTED POTENTIAL HARM IS CLASSIFIED AS SERIOUS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17625374 ↗
• MalfunctionAug 25, 2023Suction Failure; Suction Failure

  THE CUSTOMER STATED THAT THE PATIENT REQUIRED AN ADDITIONAL MEDICAL PROCEDURE (OUTSIDE THE SCOPE OF NORMAL TREATMENT). THE REPORTED POTENTIAL HARM IS CLASSIFIED AS SERIOUS.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17625139 ↗
• MalfunctionAug 25, 2023Suction Failure; Suction Failure

  PHILIPS RECEIVED A COMPLAINT ON THE NEONATAL-INFANT INTUBATED CO2 FILTER LINE, EXTENDED DURATION INDICATING A POTENTIAL NEONATAL PATIENT SAFETY ISSUE DUE TO MICROSTREAM CO2 ADAPTOR & SMITHS ET TUBE STICKING TOGETHER RESULTING IN NOT BEING ABLE TO SUCTION A CRITICALLY ILL PATIENT. SOME INSTANCES RESULTED IN A PATIENT HAVING TO BE EXTUBATED SO THAT THEY CAN BE SUCTIONED AND THE AIRWAY HAVING TO BE REINSERTED.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17624869 ↗
• MalfunctionAug 25, 2023Suction Failure; Suction Failure

  PHILIPS RECEIVED A COMPLAINT ON THE NEONATAL-INFANT INTUBATED CO2 FILTER LINE, EXTENDED DURATION INDICATING A POTENTIAL NEONATAL PATIENT SAFETY ISSUE DUE TO MICROSTREAM CO2 ADAPTOR & SMITHS ET TUBE STICKING TOGETHER RESULTING IN NOT BEING ABLE TO SUCTION A CRITICALLY ILL PATIENT. SOME INSTANCES RESULTED IN A PATIENT HAVING TO BE EXTUBATED SO THAT THEY CAN BE SUCTIONED AND THE AIRWAY HAVING TO BE REINSERTED.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17624431 ↗