# Major Recall Alert: Gore® Tag® Thoracic Branch Endoprosthesis Side Branch Component Recalled Due to Catheter Separation
Health and safety concerns have prompted the recall of the **Gore® Tag® Thoracic Branch Endoprosthesis (TBE) Side Branch (SB) Component**, a product used in critical clinical procedures. The issue stems from the **catheter separation of the Gore® Tag® TBE Side Branch during clinical use**, which could potentially lead to serious patient safety risks. If you or someone you know has been using this product, understanding the recall details and necessary actions is vital.
Below, we’ve outlined everything you need to know about this important recall and how to stay updated on similar safety alerts in the future.
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## Why This Recall is Important
Medical devices like thoracic endoprostheses are crucial for patients requiring vascular repair, particularly in the thoracic region. Any failure in these devices could have **severe implications** for patients, including procedural complications or adverse health outcomes.
The **catheter separation of the Gore® Tag® TBE Side Branch Component during clinical use** could result in:
- **Interrupted or failed procedures**
- Potential for **increased health risks** in patients
- Delayed treatment, which could worsen patient outcomes
Medical professionals should take immediate action to reduce risks to patients and evaluate alternatives if they’re using this product. The recall says it all: safety must come first, especially in life-saving procedures.
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## Details of the Recall
Here are the key facts regarding the recall of the Gore® Tag® Thoracic Branch Endoprosthesis Side Branch (TBE Side Branch) Component:
- **Brand Name**: Gore®
- **Product Name**: Gore® Tag® Thoracic Branch Endoprosthesis Side Branch Component
- **Reason for Recall**: **Catheter separation** of the side branch during clinical use.
- **Date Announced**: [Include Proper Date Format Here Once Confirmed]
- **Location Applicable**: Canada (CAN)
For complete and official information, you can visit the Health Canada recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/gorer-tagr-thoracic-branch-endoprosthesis-side-branch-component).
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## What You Should Do
If you’re a healthcare provider or patient impacted by this recall, here’s what you should do immediately:
### For Healthcare Providers:
- **Cease Use Immediately**: Stop using the **Gore® Tag® Thoracic Branch Endoprosthesis Side Branch Component** in clinical settings.
- **Notify Patients**: Inform potentially affected patients of the recall and schedule a follow-up to assess their condition.
- **Report Adverse Events**: Submit any associated issues or incidents to Health Canada.
### For Patients:
- **Contact Your Physician**: If you believe you may have been treated with this product, speak with your doctor about next steps.
- **Stay Informed**: Follow updates from Health Canada to stay aware of any further developments.
Remember, patient safety is the top priority, and timely action can save lives.
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## Stay Safe – Get Instant Recall Alerts
Keeping track of medical recalls is critical, whether you’re part of the healthcare industry or someone who relies on medical devices for your health. To make it easier to stay informed, download a health-tracking or recall alert app.
### Why Download a Recall Alert App?
- Receive **real-time notifications** for recalls.
- Get access to detailed safety information.
- Ensure you’re always informed about critical updates affecting your health.
**Act now! Stay safe and protect your health by downloading the latest recall alert app today.**
To read the official Health Canada recall notice for this product, [visit here](https://recalls-rappels.canada.ca/en/alert-recall/gorer-tagr-thoracic-branch-endoprosthesis-side-branch-component). Be proactive – your health depends on it!
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By staying vigilant about medical recalls, you can ensure the safety of yourself, your patients, or your loved ones. Share this critical information with anyone who may benefit and stay informed about future updates.