# Major Recall Alert: HistoCore PELORIS 3 Recalled Due to Reagent Leakage Issue
Leica Biosystems has issued a significant recall affecting their **HistoCore PELORIS 3 instruments**. The company has identified a reagent leakage issue linked to tubing connections in a batch of manifolds. This problem can expose operators to toxic chemicals, create potential slip hazards, and may even compromise tissue processing if leakage is severe.
If you're using the **HistoCore PELORIS 3**, it's vital to understand the impact of this recall and take immediate action. Keep reading to learn more about this critical issue and how you can stay informed about product safety updates.
## Why This Recall is Important
Leica Biosystems revealed this issue on **August 15, 2025**, following reports of reagent leaks in their **HistoCore PELORIS 3 instruments**. Their investigation showed that isolated instances of incorrectly assembled fittings caused the problem within certain batches of manifolds.
The implications of this defect include:
- **Exposure to Toxic Reagents**: Laboratory operators could be directly exposed to hazardous chemicals, potentially causing health concerns.
- **Slip Hazards**: Leaking reagents can accumulate on work surfaces and floors, creating dangerous slip-and-fall conditions.
- **Disruption to Tissue Processing**: In cases of significant leakage, the accuracy and reliability of tissue processing could be affected—potentially impacting crucial diagnostic and research work.
Understanding these risks is critical for laboratories worldwide to safeguard their personnel and ensure the continuity of their operations.
## Details of the Recall
Here’s a detailed summary of the recall:
- **Product Name**: HistoCore PELORIS 3
- **Brand**: Leica Biosystems
- **Issue**: Reagent leakage due to isolated instances of incorrectly assembled fittings in manifold tubing connections.
- **Key Risks**:
- Chemical exposure for lab operators.
- Increased slip hazards.
- Potential tissue processing impacts.
- **Recall Start Date**: August 15, 2025
- **Source**: [Official Government Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3-0)
If your facility utilizes HistoCore PELORIS 3 systems, it’s essential to verify whether your device falls under the scope of this recall and take the necessary next steps.
## What You Should Do
Leica Biosystems recommends the following actions for affected users:
1. **Inspect Your Instrument**: Check if your HistoCore PELORIS 3 is experiencing reagent leakage or matches details in the recall notice.
2. **Suspend Use Immediately**: If leakage is confirmed, stop using the instrument to prevent potential health hazards and laboratory disruptions.
3. **Contact Leica Biosystems**: Reach out to their customer support team for further assistance, including repair or replacement options.
4. **Educate Your Team**: Inform all laboratory personnel about this recall and the risks associated with continued use of the faulty devices.
By taking these precautions, laboratory managers can minimize safety hazards and operational downtime caused by this issue.
## Stay Safe – Get Instant Recall Alerts
Staying informed about the latest product recalls is crucial for maintaining workplace safety and product integrity. Protect your team and equipment by signing up for instant recall alerts on regulated products.
**Download our free app today to stay ahead of critical safety updates!** With real-time notifications and trusted information, you’ll never miss an important recall or alert.
For more details, visit the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3-0). Stay proactive, stay safe!
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This recall serves as an important reminder of how crucial it is to regularly monitor product performance and always prioritize safety in your workplace. By addressing this issue promptly, laboratories can continue performing vital research and diagnostics without compromise.