# Major Recall Alert: TEGO Connector Recalled Due to Silicone Seal Issues Identified by ICU Medical
Consumers and healthcare professionals across Canada need to be informed about the latest medical device recall affecting ICU Medical's TEGO Connector. The company has identified lot-specific issues with the silicone seal in the TEGO device, which could compromise the product's performance. This recall highlights a significant safety concern and underscores the importance of staying updated with critical health-related recalls.
For anyone using the TEGO Connector, this is what you need to know.
---
## Why This Recall is Important
The TEGO Connector plays a critical role in providing secure and effective connections in medical treatments, especially within intensive care scenarios. ICU Medical's findings about potential issues with the silicone seal of specific lots raise concerns about the efficacy and safety of this essential medical tool.
The silicone seal malfunction could pose risks such as:
- **Device failure during use**
- **Increased risk of contamination or infection**
- **Potential complications for patients reliant on its proper functioning**
Healthcare providers and patients depend on high-quality devices for critical care, and even minor defects can lead to serious implications. It is important for both medical professionals and consumers to act swiftly on this recall.
For further details about the recall, you can check the official Health Canada recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/tego-connector).
---
## Details of the Recall
Here is everything we know about the TEGO Connector recall:
- **Category:** Medical Devices (ICU Medical)
- **Product Name:** TEGO Connector
- **Brand:** TEGO Connector
- **Reason for Recall:** Lot-specific issues with the silicone seal that may affect the product’s performance.
- **Safety Concerns:** Potential risk during use, including device failure or contamination.
- **Date Announced:** [Insert Date Here]
Healthcare facilities, distributors, and individual users should remove any affected TEGO Connector products from use immediately and follow recall instructions for your safety.
---
## What You Should Do
If you're currently using or distributing the TEGO Connector, here are the steps you should take:
1. **Check Lot Numbers:** Verify if your TEGO Connector products are part of the affected lot numbers. Contact ICU Medical or refer to their documentation for further guidance.
2. **Discontinue Use:** Cease using the affected product immediately to avoid any potential complications.
3. **Follow Recall Instructions:** Adhere to the recall protocol specified by ICU Medical to return or appropriately dispose of the defective product.
4. **Consult with Healthcare Providers:** If you or your facility has used the product with patients, update your healthcare provider for monitoring or alternative treatment options.
By following these steps, you can minimize risks and ensure safety during this recall process.
---
## Stay Safe – Get Instant Recall Alerts
Staying informed about product recalls is vital, especially when it concerns your health or the health of patients under your care. To ensure you never miss a critical recall alert like this, download our app today to get instant notifications on any health-related recalls and safety concerns in Canada.
With real-time updates, user-friendly features, and reliable recall tracking, our app can help you take proactive steps to protect yourself and others.
**Don’t wait until it’s too late – [Download the App Now](#)** and stay ahead when it comes to safety.
Stay alert, stay informed, and prioritize your well-being with trusted recall updates.
---
**Source:** Visit the official recall notice from Health Canada for more information: [TEGO Connector Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/tego-connector)