# Major Recall Alert: Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recalled Due to Potential Safety Risks
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System has been officially recalled after customers reported serious issues affecting the product’s safety and functionality. The recall, announced on **March 5, 2025**, highlights two critical failure modes:
- **Bent or detached heater wire**
- **Silicone peeling or detaching from the jaws of the harvesting tool**
This recall is a precautionary measure to address these reported issues and prevent potential harm during the product’s use. Read on to learn more about the recall, why it matters, and how to take the necessary steps to mitigate risks.
---
## Why This Recall is Important
Endoscopic vessel harvesting tools, like the **Vasoview Hemopro 2**, are essential, especially in surgical procedures such as coronary artery bypass grafting. A malfunctioning device—whether due to a bent heater wire or degrading silicone materials—can pose a significant risk to patients and healthcare providers.
The reported issues have the potential to:
- **Interrupt critical surgical procedures**
- **Endanger patient safety by compromising the tool’s integrity**
- **Increase the risk of surgical errors or procedure delays**
With these risks in mind, addressing this recall promptly is vital to avoid adverse outcomes in medical settings.
---
## Details of the Recall
Customers and healthcare facilities using the **Vasoview Hemopro 2 Endoscopic Vessel Harvesting System** are urged to take action in light of the following risks:
- **Failure Modes Reported:**
- A heater wire may bend or become detached during use, leading to compromised performance.
- Silicone has shown signs of peeling or detaching from the tool’s jaws, raising concerns about durability and safe usage.
- **Recall Start Date:** March 5, 2025
Manufacturers recommend that all current users inspect their devices, follow guidance to mitigate risks, and report any abnormalities to ensure patient safety. If you own or use this product, immediate action is required.
For further details, visit the official recall alert here: [Vasoview Hemopro 2 Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/vasoview-hemopro-2-endoscopic-vessel-harvesting-system-0).
---
## What You Should Do
If you or your healthcare facility relies on the **Vasoview Hemopro 2**, follow these steps to ensure safety:
- **Inspect the Device:** Check for any signs of wear, including bent wires or silicone peeling.
- **Contact the Manufacturer:** Report any issues and request guidance on replacement or repair options.
- **Cease Use if Defects Are Found:** Avoid using the product until you’ve consulted with the manufacturer or received a resolution.
- **Spread the Word:** Raise awareness among colleagues or institutions who may also use the product.
By acting quickly, you can help ensure patient safety and maintain the integrity of surgical procedures.
---
## Stay Safe – Get Instant Recall Alerts
Recalls like this one demonstrate the importance of staying informed about product issues that could impact safety and effectiveness. Don’t miss critical updates—download our free recall alert app to:
- Receive **instant notifications** about new recalls
- Access detailed recall information, including safety measures and next steps
- Stay ahead of potential risks in your personal or professional life
[**Click here to download the app now**](https://myrecalls.app)!
---
The **Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall** reminds us of the importance of proactive device safety monitoring and prompt action. For the latest updates, always consult official sources like the [Government of Canada Recall Database](https://recalls-rappels.canada.ca/en/alert-recall/vasoview-hemopro-2-endoscopic-vessel-harvesting-system-0). Stay informed, stay safe!