Trilogy Evo O2 and Trilogy Evo Portable Ventilators

Official notice

8 Oct 2021

Last checked

8 Oct 2021

Medium riskACCC

An official ACCC notice concerns Trilogy Evo O2 and Trilogy Evo Portable Ventilators. 1. Infant/Pediatric EFS Calibration Pressure Increase Potential for inappropriate therapy to be provided when the EFS is used with manual calibration, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Hypercarbia (too much carbon dioxide in the blood) 2. Issue 2 – Pressure Drift (Continuous Usage) Potential for inappropriate therapy to be provided to a patient if there is a pressure increase or decrease from the baseline pressure settings without alarm, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Dyspnea (a sensation of shortness of breath) - Hypoxemia (a low amount of oxygen in the blood) Published 2021-10-08.

What to do now

Philips will be releasing a software correction for this issue. Philips will be contacting customers when the software is released. In the interim, customers are advised to refer to the steps provided in the Customer Letter (supplied to impacted users by Philips) until the updated software is installed on the device. Infant/Pediatric EFS Calibration Pressure Increase If you are using the infant/pediatric EFS, do not perform a manual circuit calibration. Instead, use the default calibration. The pressure increase will not occur if the default circuit calibration is used. Pressure Drift (Continuous Usage) If a pressure drift is detected, the decision to reset the device and return to its original, intended settings MUST be made in consultation with a clinician. Take steps to support the patient during a brief interruption in therapy, as needed. For further information, consumers should contact Philips Customer Care Centre by phone on 1800 251 400.

Recall number

ecf82957-b64a-4c6d-9237-551d9ba4e009

Official notice

2021-10-08

The hazard

1. Infant/Pediatric EFS Calibration Pressure Increase Potential for inappropriate therapy to be provided when the EFS is used with manual calibration, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Hypercarbia (too much carbon dioxide in the blood) 2. Issue 2 – Pressure Drift (Continuous Usage) Potential for inappropriate therapy to be provided to a patient if there is a pressure increase or decrease from the baseline pressure settings without alarm, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Dyspnea (a sensation of shortness of breath) - Hypoxemia (a low amount of oxygen in the blood)

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

list

Models

IS USED CONTINUOUSLY WITHOUT ANY INTERRUPTION TO THERAPY

Artg Numbers

332200

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Affected products

Product 1

Trilogy Evo O2 and Trilogy Evo Product codes: IN2100X15B and IN2110X15B Multiple serial numbers (see attached serial number list) ARTG 332200 (Philips Electronics Australia Ltd - Portable ventilator, electric)

Risk / hazard

1. Infant/Pediatric EFS Calibration Pressure Increase Potential for inappropriate therapy to be provided when the EFS is used with manual calibration, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Hypercarbia (too much carbon dioxide in the blood) 2. Issue 2 – Pressure Drift (Continuous Usage) Potential for inappropriate therapy to be provided to a patient if there is a pressure increase or decrease from the baseline pressure settings without alarm, increasing the risk of serious health complications including: - Barotrauma (an injury to the lungs because of too much pressure) - Hypotension (a decrease in blood pressure) - Dyspnea (a sensation of shortness of breath) - Hypoxemia (a low amount of oxygen in the blood)

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

AU · Australia

Affected area 1

AU · Australia

Source & status

Source

Tier

beta

Category

HOME

Classification

Pharmacy and medical products

App estimate

medium

Recall details

Recall number

ecf82957-b64a-4c6d-9237-551d9ba4e009

Classification

Pharmacy and medical products

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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