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Philips Respironics, Inc. Recalls Trilogy Evo Ventilators due to Software-Related Possible Power Malfunction

Please be aware, this recall is a correction, not a product removal. 

Philips Respironics, Inc. notified customers to update to the latest software version (1.05.06.00) for its Trilogy Evo continuous ventilators due to a software-related possible power malfunction. Due to the software issue, these ventilators may issue a “Battery Depleted” or “Loss of Power” alarm while sufficient power is still available. This issue may result in a sudden loss of ventilation while the device alarms.

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. 

Questions?

If you have questions about this recall, contact Philips Respironics at 1-800-345‐6443 for homecare customers or 1-800-722‐9377 for hospital customers.