# Major Recall Alert: Airvo™ 2 Humidifier and myAirvo™ 2 Humidifier Disinfection Kit Manual Updated for Safety Concerns
If you own the **Airvo™ 2 Humidifier** or **myAirvo™ 2 Humidifier**, take note of this important recall update. The disinfection kit user manual has been updated to include a mandatory **test of the device's audible alert** to ensure safe operation during patient use. This is a critical safety measure to maintain the functionality and reliability of your device throughout its service life.
Read on to learn why this recall was issued, what it means for you, and the steps you should take to stay safe.
## Why This Recall is Important
The **Airvo™ 2 Humidifier** and **myAirvo™ 2 Humidifier** are trusted medical devices designed to provide humidification therapy for patients in various medical settings. These devices feature an audible alert that activates for a minimum of 120 seconds if unintentionally disconnected from a power source.
However, Fisher & Paykel Healthcare has reported instances where this alert may **sound for less than 120 seconds**, potentially delaying user awareness of power disconnection. While no injuries or fatalities have been associated with this issue, this recall emphasizes proactive safety through user testing and device maintenance to avoid future risks.
## Details of the Recall
Here is what you need to know about the **Airvo™ 2 Humidifier** and **myAirvo™ 2 Humidifier** recall:
- **Recall Category**: Canada (CAN)
- **Affected Products**: Airvo™ 2 Humidifier and myAirvo™ 2 Humidifier
- **Reason**: Update to the disinfection kit user manual; includes a new requirement to test the 120-second audible alert between patient uses.
- **Date of Recall Start**: August 27, 2025
- **Safety Concern**: The audible alert may sound for **less than 120 seconds** when the device is disconnected from power, potentially delaying user response time for reconnection.
- **Serious Incidents Reported**: None as of the recall announcement.
For additional details, you can review the official announcement from the **Government of Canada** [here](https://recalls-rappels.canada.ca/en/alert-recall/myairvotm-2-and-airvotm-2-humidifier).
## What You Should Do
If you own or operate the **Airvo™ 2 Humidifier** or **myAirvo™ 2 Humidifier**, follow these steps to ensure the safety and proper functioning of your device:
1. **Update Procedures**: Refer to the updated disinfection kit user manual provided by Fisher & Paykel Healthcare. This document now includes protocols for regular testing of the audible alert.
2. **Test Audible Alerts**: Between patient uses, test the system's audible alert to verify proper functionality. If the alarm does not sound for the required **120 seconds**, contact Fisher & Paykel for further support.
3. **Stay Informed**: Register your device, if applicable, to receive any related updates directly from the manufacturer.
4. **Reach Out for Help**: For assistance or questions, contact Fisher & Paykel Healthcare directly through their customer service channels.
## Stay Safe – Get Instant Recall Alerts
Ensuring the proper maintenance and operation of medical equipment like the **Airvo™ 2 Humidifier** or **myAirvo™ 2 Humidifier** is critical for patient safety. Don’t miss important updates like this – download the **MyRecalls App** today to receive real-time notifications on product recalls that matter to you!
Stay ahead of safety concerns by quickly responding to recalls in your region. To learn more about this specific recall, visit the official page of the **Government of Canada Recall Database**: [myAirvo™ 2 and Airvo™ 2 Humidifier Recall Details](https://recalls-rappels.canada.ca/en/alert-recall/myairvotm-2-and-airvotm-2-humidifier).
Your safety is important – act now to ensure your medical devices are operating as intended!
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