Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine and FilterLine® Intubated CO2 Filter Line
Brand(s)
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Filterline Set H Infant/Neonatal |
Not applicable. |
9898031 60261 |
Filterline Set Adult/Pediatric |
Not applicable. |
M1920A |
Filterline Set H Adult/Pediatric |
Not applicable. |
M1921A |
Filterline Set H Adult/Pediatric |
Not applicable. |
9898031 59571 |
Filterline Set H Infant/Neonatal |
Not applicable. |
9898031 59581 |
Issue
The supplier of the Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine and FilterLine® Intubated CO2 Filter Line has provided an update to the instructions for use (IFU) for affected product. The IFU addendum is being issued to address customer reports of difficulty or inability to disconnect an adapter from a patient's endotracheal tube in order to perform a procedure. The addendum includes information on potential adverse events that may result from a failure to follow instructions for safe use of the airway adapter, as originally stated in the IFU.
Recall start date: April 15, 2025
Additional information
Details
Philips Medical Systems
3000 Minuteman Road, Andover, Massachusetts, United States, 01810
Get notified
Receive emails about new and updated recall and safety alerts.