# Major Recall Alert: Leica Biosystems Issues HistoCore PELORIS 3 Recall Over Leakage Hazard
Leica Biosystems has issued a significant product recall for their **HistoCore PELORIS 3 instrument** due to a critical safety issue. The company identified a leakage associated with the tubing in the manifold of the instrument, which could expose operators and laboratory personnel to toxic chemicals and create slip hazards in laboratory environments. The recall officially began on **April 2, 2025**, and affected users are urged to take immediate action to mitigate safety risks.
Read on to discover why this recall is critical, the specific concerns, and the steps you should take to stay safe.
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## Why This Recall is Important
Leica Biosystems’ **HistoCore PELORIS 3** is a widely-used tissue processor in medical and laboratory settings. It plays a vital role in diagnosing and studying diseases, making its reliability crucial. The issue identified in the manifold tubing of the device is particularly alarming due to the potential hazards:
- **Toxic exposure risk**: Leakage of chemicals may endanger the health of laboratory staff by exposing them to harmful toxins.
- **Slip hazard**: Leaked chemicals can create slick surfaces, increasing the likelihood of accidents and workplace injuries.
Given the significant safety implications, Leica Biosystems has prioritized drawing attention to this recall to ensure user safety.
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## Details of the Recall
Below are the key details you need to know about this recall:
- **Brand**: HistoCore PELORIS 3
- **Product**: Advanced Tissue Processor used in laboratory environments
- **Reason for Recall**: Leakage in the manifold tubing, potentially exposing operators to toxic chemicals and creating a slip hazard.
- **Recall Start Date**: April 2, 2025
- **Official Source Link**: [Check the Recall Notice Here](https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3)
This recall applies to all units of the HistoCore PELORIS 3. If your laboratory relies on this specific instrument, it’s crucial to pause usage immediately and follow the outlined safety measures.
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## What You Should Do
If your facility owns the Leica Biosystems **HistoCore PELORIS 3**, here’s what you need to do:
1. **Discontinue Use Immediately**: To eliminate potential risks of toxic exposure or accidents, pause operations using this system.
2. **Inspect Affected Units**: Conduct a thorough inspection of the tubing and manifold for signs of leakage or potential hazards.
3. **Contact Leica Biosystems**: Reach out to the manufacturer for further instructions, repair services, or replacement options.
4. **Inform Staff**: Make sure all laboratory personnel are aware of the recall, potential hazards, and importance of avoiding use until the issue is fixed.
5. **Visit the Official Recall Page**: Access the official notice [here](https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3) for comprehensive information.
Taking immediate action can protect your team and prevent accidents in your laboratory.
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Product safety should never be compromised. With the **HistoCore PELORIS 3 recall**, Leica Biosystems is taking the necessary steps to address these concerns. Laboratory professionals are urged to act quickly to ensure a safe environment for everyone involved. For more details, visit the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3).
Stay informed, stay safe, and take swift action today!