# Major Recall Alert: EVIS EXERA III Duodenovideoscope Recalled Due to Updated Reprocessing Instructions
Olympus has issued an important update for the reprocessing materials of its **EVIS EXERA III Duodenovideoscope**, aiming to minimize potential deviations in TJF duodenoscope reprocessing. This critical recall emphasizes the need for healthcare providers to follow updated reprocessing protocols to ensure patient safety. Users of the affected product must review the latest materials, available through Olympus' education portal, and acknowledge their understanding to comply with the changes.
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## Why This Recall is Important
This recall is critical as it directly impacts the reprocessing of the **EVIS EXERA III Duodenovideoscope**, a specialized device used in endoscopic procedures. Proper reprocessing is essential to prevent cross-contamination and ensure patient safety. Deviations in cleaning and reprocessing protocols could pose a significant risk of infection during medical procedures.
Olympus’ updated materials are designed to address and minimize any potential deviations that could occur during the device’s reprocessing. By ensuring that users adhere to the new guidelines and remind them of safe handling and operation, Olympus is prioritizing patient safety and the reliability of their medical devices.
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### Details of the Recall
Here’s a breakdown of the key information regarding this recall:
- **Product Category**: Medical devices for endoscopy
- **Brand**: Olympus
- **Model**: **EVIS EXERA III Duodenovideoscope**
- **Reason for Recall**: Updated reprocessing materials to address potential deviations in TJF duodenoscope reprocessing protocols.
- **User Action Required**:
1. Carefully review all updated reprocessing instructions available through Olympus' education portal.
2. Acknowledge reviewing the materials to comply with the recall update.
3. Follow the revised reprocessing steps for the safe and effective handling of the device.
- **Date Announced**: October 2023
- **Impact**: Ensures patient safety by addressing potential contamination risks.
For the official recall notice, visit: [Canada Recalls and Alerts – EVIS EXERA III Duodenovideoscope](https://recalls-rappels.canada.ca/en/alert-recall/evis-exera-iii-duodenovideoscope-1).
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### What You Should Do
If you or your facility uses the **EVIS EXERA III Duodenovideoscope**, follow these steps immediately:
1. **Access Olympus’ Education Portal**: Log in to the portal to view the updated reprocessing materials.
2. **Review Updated Instructions**: Read through the revised protocols to familiarize yourself with the changes.
3. **Acknowledge Completion**: Confirm that you have reviewed and understood the materials as directed by Olympus.
4. **Implement the Changes**: Ensure that all staff handling and reprocessing the duodenoscope adhere to the new instructions.
If you have questions or need further clarification, contact Olympus’ customer support team for assistance.
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### Stay Safe – Get Instant Recall Alerts
In an ever-evolving medical landscape, staying informed about product updates and recalls is vital to maintaining patient safety and regulatory compliance. Download our **Recall Alerts App** today to receive instant notifications for critical recalls like this one.
With the app, you can:
- Access real-time updates on product recalls in Canada.
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Your commitment to patient care starts with staying informed. Download the app now and safeguard your practice from potential risks.
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**Your Safety Matters**
Act immediately by reviewing Olympus' updated instructions to address this recall. For further information, visit the official recall page [here](https://recalls-rappels.canada.ca/en/alert-recall/evis-exera-iii-duodenovideoscope-1). Stay safe and informed!