# Major Recall Alert: Medtronic Airway Adapters Recall for Adult/Pediatric and Infant/Neonatal Products Due to Detachment Issues
Medtronic has announced an important recall starting February 19, 2025, involving its **Airway Adapter, Adult/Pediatric, CO2 Sampling Line, Filterline H Set** (and related products). This action follows reports of **difficulty or inability to disconnect the adapters from endotracheal tubes** during medical procedures. It is essential for healthcare professionals and caregivers to be informed of this update to ensure patient safety. Keep reading for detailed information on the recall, why it matters, and what steps you need to take.
## Why This Recall is Important
Patient safety is the top priority in medical procedures, and the proper functionality of airway adapters is critical in respiratory care. There have been concerning reports highlighting issues with certain Medtronic airway adapter models, where **adapters cannot be easily detached from breathing circuits or endotracheal tubes.**
This issue can pose a serious risk to patients, especially in emergency situations where prompt disconnection is necessary to perform lifesaving interventions. According to Medtronic's updated **Instructions for Use (IFU)**, healthcare providers must ensure that adapters can **easily attach and detach** from breathing circuits or tubing before use.
The recall and IFU update aim to mitigate risks associated with these devices and improve their safe and effective use in clinical settings.
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## Details of the Recall
Here is an overview of the key details regarding the recall:
- **Category**: Medical devices (Adult/Pediatric and Infant/Neonatal airway adapters)
- **Brand/Models Affected**:
- **Airway Adapter, Adult/Pediatric, CO2 Sampling Line**
- **Filterline H Set** (Adult/Pediatric, Infant/Neonatal, Long)
- **Filterline Set** (Long, Adult/Pediatric)
- **Omni Ventline Set**
- **Vitaline H Set** (Adult/Pediatric, Infant/Neonatal)
- **Problem Identified**:
Issues with **difficulty or inability to disconnect the adapter from patients' tubes** during medical procedures.
- **Recall Start Date**: February 19, 2025
- **Official Source**: [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/infantneonatal-and-adultpediatric-filterline-and-vitaline-h-sets-airway-adapters)
To enhance safety protocols, Medtronic advises following the updated **Instructions for Use (IFU)**. During pre-procedure setup, confirm that the adapter can be attached and detached before proceeding with treatment.
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## What You Should Do
If you are using any of the recalled Medtronic airway adapter products, follow these steps to ensure compliance and patient safety:
1. **Verify IFU Updates**
Carefully review and adhere to the updated instructions provided by Medtronic. Make sure the airway adapter can be easily connected and disconnected at the setup stage.
2. **Identify Affected Products**
Check your inventory for the model names and product details provided above.
3. **Contact Medtronic**
If you experience issues or have concerns, contact Medtronic for further guidance and support on how to replace or resolve impacted devices.
4. **Report Any Issues**
Healthcare professionals should report incidents related to these products to their local health authority.
For more information, consult the official recall notice: [Medtronic Airway Adapter Recall Information](https://recalls-rappels.canada.ca/en/alert-recall/infantneonatal-and-adultpediatric-filterline-and-vitaline-h-sets-airway-adapters).
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## Stay Safe – Get Instant Recall Alerts
Staying informed about medical recalls is critical to safeguarding the well-being of patients and ensuring compliance with updated safety standards. Ensure you never miss an important recall announcement by downloading the **MyRecalls app.**
With **MyRecalls**, you can:
- Receive instant alerts for product recalls in your region.
- Access detailed information about affected products.
- Stay updated with the latest safety measures and recommendations.
**[Download the MyRecalls App Today](https://myrecalls.app)** and take control of safety in your healthcare environment. Trust us to keep you informed and prepared!
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In summary, the Medtronic airway adapter recall is a call to action for enhanced vigilance and adherence to updated guidelines. Prioritize patient safety by reviewing IFU updates and taking the necessary steps to minimize risks in clinical practice.