Health product recall

Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine and FilterLine® Intubated CO2 Filter Line

Last updated

Summary

Product
Microstream™ Advance Intubated CO2 Filter Line, VitaLine® Intubated CO2 FilterLine and FilterLine® Intubated CO2 Filter Line
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
Filterline Set H Infant/Neonatal Not applicable. 9898031 60261 M1923A
Filterline Set Adult/Pediatric Not applicable. M1920A 9898031 60241
Filterline Set H Adult/Pediatric Not applicable. M1921A 9898031 60251
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
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies

Philips Medical Systems

3000 Minuteman Road, Andover, Massachusetts, United States, 01810

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77349

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe