# Major Recall Alert: Heartstring III Proximal Seal System Recalled Due to Critical Safety Issues
The **Heartstring III Proximal Seal System**, a widely used medical device designed for cardiac surgery, has been **recalled as of August 14, 2025**, due to three significant failure modes. The recall arises from concerns regarding the seal's ability to function correctly during use, which can pose serious health risks. If you or a loved one rely on this product, it's crucial to understand the issue and take immediate action to ensure safety.
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## Why This Recall is Important
The **Heartstring III Proximal Seal System** is a critical tool in cardiac surgeries, designed to create a sealed environment and maintain proper blood flow during procedures. However, the manufacturer has identified **three primary failure modes** that undermine the device's reliability:
- **Failure of the heartstring seal to load properly**
- **Failure of the heartstring seal to deploy within the aortotomy**
- **Failure of the deployed seal to ensure adequate hemostasis (stop bleeding)**
Given that cardiac surgeries require precision and depend entirely on reliable equipment, these failures could lead to excessive bleeding, procedural complications, or life-threatening situations. Public health and safety are at the forefront of this recall, making it critical for healthcare providers and patients to act swiftly.
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## Details of the Recall
To ensure complete transparency, here’s what we know so far:
- **Product Name**: Heartstring III Proximal Seal System
- **Brand**: Heartstring III Proximal Seal System
- **Issue**: Identified failure modes compromising the safety and functionality of the device.
- Seal fails to load
- Seal fails to deploy properly into the aortotomy
- Seal fails to maintain adequate hemostasis after deployment
- **Recall Date**: August 14, 2025
- **Impact**: Potential risks include surgical complications, emergencies, and extended recovery time for patients.
For further details, you can find the official recall announcement here: [Canada Recall Notice – Heartstring III Proximal Seal System](https://recalls-rappels.canada.ca/en/alert-recall/heartstring-iii-proximal-seal-system).
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## What You Should Do
If you or your healthcare provider uses the Heartstring III Proximal Seal System, here are the immediate steps you should take:
1. **Verify the Product**: Confirm if the device you’re using is part of the recall. Check the device’s labeling and serial numbers against details provided in the official recall notice.
2. **Contact the Manufacturer**: Reach out for guidance on product returns, exchanges, or refunds. The manufacturer should provide instructions for disposing of or replacing the product.
3. **Consult Your Healthcare Provider**: If you’ve had cardiac surgery where this system was used, inform your provider to discuss potential health monitoring or any necessary follow-up care.
4. **Stay Updated**: Ensure you monitor official sources for updates on corrective measures or further recalls.
Delays in addressing this issue could have severe consequences. Taking proactive steps now can help protect your health or that of a loved one.
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## Stay Safe – Get Instant Recall Alerts
In today’s fast-paced world, staying informed about important recalls can be a challenge. Don’t leave your health or safety to chance. Download our app to receive **real-time updates on recalls** like the Heartstring III Proximal Seal System.
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For more information on this recall, visit the official notice here: [Canada Recall Notice – Heartstring III Proximal Seal System](https://recalls-rappels.canada.ca/en/alert-recall/heartstring-iii-proximal-seal-system).
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**Final Note**: Your health and safety are paramount. If you have additional questions, contact the manufacturer or your healthcare professional for guidance. Stay vigilant, and take immediate action to ensure your well-being.