Trilogy EV300
Last updated
Summary
Product
Trilogy EV300
Issue
Medical devices - Sterility Issue
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected product |
Lot or serial number |
Model or catalog number |
|---|---|---|
Trilogy EV300 |
All lots. |
CA2200X12B |
Issue
Philips Respironics has detected environmental contamination (e.g. External dust and dirt) in the air path of some devices that have been returned from the field. Extended exposure to these environmental contaminants can lead to buildup of particulate on a flow sensor within the device. This may cause the device to inaccurately deliver pressure or volume/flow.
Recall start date: April 6, 2023
Additional information
Details
Original published date: 2023-05-10
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies
Respironics Inc. Also Trading As Philips Rs North America LLC
1001 Murry Ridge Lane, Murrysville, Pennsylvania, United States, 15668
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-73639