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Monnal™ T60 Advanced Recall Due to Air Liquide Medical Systems has identified...

# Major Recall Alert: Monnal™ T60 Advanced Recalled Due to Manufacturing Non-Conformity

Air Liquide Medical Systems has issued a critical recall affecting specific Monnal™ T60 and Monnal™ T60 Advanced devices. The issue? A manufacturing non-conformity that could compromise the safety and compliance of these devices, particularly for medical use in air and road ambulances. This recall highlights the importance of rigorous quality standards in medical devices.

If you or your organization uses the Monnal™ T60 Advanced, here’s everything you need to know and how you can take action immediately.

## Why This Recall is Important

The Monnal™ T60 Advanced is a high-performance medical device relied upon by emergency healthcare providers, especially in air and road ambulances. However, due to a manufacturing defect identified by Air Liquide Medical Systems, vital washers were not fitted beneath the screw head securing the inspiratory unit of the device.

The absence of these washers raises serious concerns regarding the device’s compliance with two key medical standards:
- **EM 13718-1**: Specifies requirements for medical devices used in air ambulances.
- **EN 1789+A1**: Outlines standards for medical devices used in road ambulances.

Non-compliance to these standards could pose safety risks to healthcare providers and patients who rely on the Monnal™ T60 for lifesaving treatments during emergency transport.

## Details of the Recall

Here are the key details of the Monnal™ T60 Advanced recall:

- **Category**: Medical Equipment Recall
- **Brand**: Monnal™ T60 Advanced
- **Product**: Monnal™ T60 & Monnal™ T60 Advanced
- **Reason for Recall**: Failure to install washers under the screw head securing the inspiratory unit.
- **Implications**: Non-compliance with EM 13718-1 and EN 1789+A1 standards for medical devices in ambulances.
- **Date Announced**: October 2023
- **Official Source for Information**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/monnaltm-t60-advanced)

If your healthcare facility or service uses these devices, immediate attention and action are required to ensure safety and compliance.

## What You Should Do

To safeguard patient care and medical standards, follow these steps if you’re affected by this recall:

1. **Identify Affected Units**: Check the model and serial numbers of your Monnal™ T60 Advanced devices. Verify if they fall within the recall scope.
2. **Contact Air Liquide Medical Systems**: Reach out to the company directly for further instructions on how to proceed with inspections or replacements.
3. **Cease Usage if Necessary**: If a device is found to be non-compliant or defective, immediately stop usage to prevent potential risks during emergency operations.
4. **Stay Updated**: Regularly check the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/monnaltm-t60-advanced) for additional updates or instructions.

Your proactive response is crucial to maintaining the safety and effectiveness of emergency medical care.

## Stay Safe – Get Instant Recall Alerts

Recalls like these underscore the importance of staying informed, especially when it comes to critical medical equipment. By downloading recall alert apps or subscribing to official alerts, you can receive real-time notifications about product recalls that may affect you or your organization.

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For more details on the Monnal™ T60 Advanced recall, visit the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/monnaltm-t60-advanced). Stay informed, act quickly, and prioritize safety—because when it comes to healthcare, there’s no room for compromise.

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