# Major Recall Alert: Pentax Medical Video Processor Recalled Due to Potential Patient Risks
Pentax Medical has issued a significant recall for their **EPK-i8020c video processor** and **i20c series video endoscopes**, utilized in endoscopic procedures. The recall, which began on **August 4, 2025**, highlights potential risks observed during device use. While no severe incidents have been reported, medical professionals and facilities should take immediate action to avoid potential risks to both patients and staff.
This recall emphasizes the importance of vigilance and immediate response when it comes to medical device safety. Below, you'll find all pertinent details about the recall and necessary steps to take to protect patients.
## Why This Recall is Important
Medical procedures rely on advanced devices like the Pentax Medical Video Processor to ensure effective diagnostics and treatment. However, under specific conditions, this equipment may pose risks:
- **Image Quality Issues**: During endoscopic procedures, images from the device may become **reddish or dark**, potentially impacting diagnostic accuracy.
- **Overheating Light Guide**: The light guide at the device tip may become **hot during use or after removal**, posing a thermal hazard to patients.
- **Steam-Like Vaporization**: Steam or vapor may be observed during procedures, raising safety concerns for medical teams.
While no severe injuries have been reported, these issues underline the need for swift precautionary measures to maintain patient safety.
## Details of the Recall
Here’s everything you need to know about the recall:
- **Product Category**: **Video processors and video endoscopes**
- **Brand**: **Pentax Medical**
- **Products Affected**: Pentax Medical **EPK-i8020c Video Processor** and **i20c Series Video Endoscopes**
- **Recall Reason**:
- Red/discolored or darkened images during procedures.
- Hot light guide tips posing a burn hazard to patients.
- Steam observation during procedures, presenting a patient and staff safety concern.
- **Recall Start Date**: **August 4, 2025**
- **Official Source**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/pentax-medical-video-processor)
## What You Should Do
If your facility utilizes the affected Pentax Medical equipment, follow these steps immediately:
1. **Stop Using Affected Devices**: Discontinue the use of the EPK-i8020c video processor and i20c series endoscopes.
2. **Contact Pentax Medical**: Reach out to the manufacturer for further instructions on device inspection, service, or replacement.
3. **Report Incidents**: If you encountered overheating or other device issues during use, report them to Health Canada or Pentax Medical.
4. **Inform Teams**: Ensure all medical staff are aware of the recall to prevent accidental use of the equipment during procedures.
Quick action can prevent potential harm to patients and staff while supporting smoother resolution efforts with the manufacturer.
## Stay Safe – Get Instant Recall Alerts
Staying on top of medical device recalls is crucial to patient safety. Download the **[MyRecalls App](https://myrecalls.app)** to receive **real-time alerts** for product recalls, medical devices, and safety notices. Stay informed, take quick action, and protect those you serve.
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For more information on this recall, visit the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/pentax-medical-video-processor).