# Major Recall Alert: Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recalled Due to Ceramic C-Ring Breakage Concern
A critical recall has been issued for the **Vasoview Hemopro 2 Endoscopic Vessel Harvesting System**, starting **March 31, 2025**, due to concerns over the **Ceramic C-ring** potentially breaking while in use. This recall impacts devices manufactured between **November 5, 2024, and February 14, 2025**, and aims to inform medical professionals through a **Field Safety Notification (FSN)**.
Keep reading to learn more about this recall, why it's crucial, and what actions you should take to ensure safety.
## Why This Recall is Important
The **Vasoview Hemopro 2 Endoscopic Vessel Harvesting System** plays an essential role in medical procedures, particularly in **endoscopic vein harvesting during coronary artery bypass graft surgeries**. However, a defect in the **Ceramic C-ring** poses potential dangers such as:
- **Breakage during use**, which may lead to delays in critical procedures.
- **Risk to patient safety**, as the malfunction may result in surgical complications or the need for alternative tools.
Medical professionals and healthcare institutions must take this recall seriously to avoid potential risks in their operating environments.
## Details of the Recall
The following key details outline the scope of this recall:
- **Product Name**: Vasoview Hemopro 2 Endoscopic Vessel Harvesting System
- **Recall Reason**: The Ceramic C-ring in certain units has a potential to break while in use.
- **Impacted Devices**: Only units manufactured between **November 5, 2024, and February 14, 2025**.
- **Recall Start Date**: March 31, 2025
- **Action Being Taken**: Distribution of a **Field Safety Notification (FSN)** with detailed guidelines for affected customers.
To visually identify the affected product, refer to the supplied image:
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For further official details, visit the [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/vasoview-hemopro-2-endoscopic-vessel-harvesting-system-1).
## What You Should Do
If you own or use the **Vasoview Hemopro 2 Endoscopic Vessel Harvesting System**, here’s what you need to do immediately:
- **Check the manufacturing date** of your device. The recall applies only to units produced between **November 5, 2024, and February 14, 2025**.
- **Discontinue use** of affected devices to avoid potential procedural risks.
- **Contact the manufacturer** for detailed instructions on handling or replacing impacted units.
- Review the distributed **Field Safety Notification (FSN)** for important safety guidance.
By taking these proactive steps, you can help mitigate patient safety risks and comply with the recall requirements.
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This **Vasoview Hemopro 2 recall notification** serves as an important reminder to regularly monitor the status of your medical equipment and stay up-to-date on safety alerts. For more details regarding the recall, visit [Health Canada’s official source](https://recalls-rappels.canada.ca/en/alert-recall/vasoview-hemopro-2-endoscopic-vessel-harvesting-system-1). Prioritize patient and practitioner safety with timely action!