Health product recall

Trilogy EVO and EV300

Last updated

Summary

Product
Trilogy EVO and EV300
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare
Industry

Affected products

Affected products

Lot or serial number

Model or catalog number

Trilogy EVO

Not applicable.

CA2110X12B

Trilogy EV300

Not applicable.

CA2200X12B

Issue

Philips Respironics has become aware of a potential safety issue with Trilogy EVO and Trilogy EV300 devices where the ventilator can issue a battery depleted or loss of power alarm while sufficient power is still available.  This can result in a sudden loss of ventilation while the device alarms. A  software algorithm that calculates remaining battery life can malfunction and cause the device to either: 

1. Issue a loss of power alarm that stops CPAP or PSV therapy while operating on battery power alone. 

2. Issue a battery depleted alarm while continuing therapy if plugged into a permanent power source. 

 

Recall start date: March 4, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies

Philips Electronics Ltd.

1875 Buckhorn Gate, Mississauga, Ontario, Canada, L4W 5P1

 

Respironics Inc. Also Trading As Philips Rs North America Llc

1001 Murry Ridge Lane, Murrysville, Pennsylvania, United States, 15668

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-75281

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