Product Wiki · Recalls · Health Canada — Medical Devices

Trilogy EVO and EV300 — recall 75281

Health Canada — Medical Devices · Canada · 2024-03-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
75281
Date of alert
2024-03-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Anaesthesiology
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/trilogy-evo-and-ev300

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.