# Major Recall Alert: Ventilator Circuit For Non-Invasive Ventilation Recalled Due to Risk of Tubing Separation
Armstrong Medical LTD has issued a critical recall for its **Ventilator Circuit for Non-Invasive Ventilation** devices. The company has also released a Field Safety Corrective Action (FSCA) report and Field Safety Notice (FSN) to address a serious issue: **the risk of tubing separation from the purple cuff connector.** The affected devices will undergo updates to the Instructions for Use (IFU) to include new warnings and detailed instructions for users to ensure safe operation. This recall has significant implications for healthcare providers and must not be overlooked.
For an official notification, visit the source: [Government of Canada Recall Alert](https://recalls-rappels.canada.ca/en/alert-recall/ventilator-circuit-non-invasive-ventilation).
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## Why This Recall is Important
Patient safety must always be the top priority, particularly for medical devices like ventilator circuits that assist non-invasive ventilation. Armstrong Medical LTD has identified **a critical design flaw that poses potential risks to patients**:
- **Tubing Separation Hazard**: The purple cuff connector in certain devices may separate from the tubing, potentially disrupting airflow and ventilation therapy.
- **Patient Safety Concerns**: Any disruption or malfunction in ventilation circuits can lead to serious health consequences, particularly for those relying on non-invasive ventilators for respiratory support.
With this recall, the company is taking proactive steps to correct the issue, update device usage instructions, and mitigate further risks.
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### Details of the Recall
Here’s what you need to know about this recall:
- **Product Name**: Ventilator Circuit For Non-Invasive Ventilation
- **Brand**: Armstrong Medical LTD
- **Reason for Recall**: Tubing separation risk involving the purple cuff connector.
- **Corrective Measures**: Updated warnings and instructions will be added to the product’s Instructions for Use (IFU).
- **Date Announced**: October 2023
- **Recall Type**: Field Safety Corrective Action (FSCA) + Field Safety Notice (FSN)
For additional specifics or concerns, healthcare providers and consumers can visit the official recall alert linked above.
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### What You Should Do
If you or a healthcare facility uses Armstrong Medical LTD’s **Ventilator Circuit for Non-Invasive Ventilation**, it is imperative to act quickly:
1. **Identify the Device**: Cross-reference your ventilator circuits with the list of affected devices in the FSN.
2. **Follow Manufacturer Guidelines**: Adhere to updated warnings and usage instructions in the revised IFU as soon as they are issued.
3. **Contact the Manufacturer**: Directly reach out to Armstrong Medical LTD for support, device corrections, or replacements.
4. **Report Any Incidents**: If you’ve experienced tubing separation or related issues, file a report with health authorities in accordance with local regulatory guidelines.
Additionally, healthcare facilities are encouraged to train staff on updated product instructions to prevent potential risks.
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### Stay Safe – Get Instant Recall Alerts
In today’s fast-paced world, keeping track of product recalls can be challenging. Stay informed and protect your family or patients by downloading the **MyRecalls app**.
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Safety is a shared responsibility, and timely action can save lives. Stay informed, adhere to recall instructions, and ensure the well-being of those relying on these vital medical devices.
For more information, check out the official recall announcement: [Ventilator Circuit Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/ventilator-circuit-non-invasive-ventilation).