# Major Recall Alert: OER-PRO Endoscope Reprocessor Recalled Due to Fire-Related Incident
Olympus has issued a significant safety alert concerning its **OER-PRO Endoscope Reprocessor**, a device widely used in medical facilities for cleaning and disinfecting endoscopes. This recall follows a **fire-related incident** involving the product. Olympus is urging all users of its endoscope reprocessors to carefully review the **warnings, cautions, and inspection guidelines** detailed in the product’s operational manual to prevent potential risks.
In this post, we’ll detail the importance of this recall, what steps users should take, and how you can stay informed about safety recalls to protect your team and patients.
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## Why This Recall is Important
Device safety in healthcare is paramount, as the performance of these tools directly impacts patient care and facility operations. The recall of the **OER-PRO Endoscope Reprocessor** is particularly critical due to the following reasons:
- **Potential Fire Hazards**: The fire-related issue reported poses a serious safety threat to staff, patients, and healthcare facilities.
- **Widespread Use in Healthcare Settings**: The OER-PRO is a commonly used device for disinfecting endoscopes, making this an issue with broad implications throughout hospitals, clinics, and outpatient centers.
- **Preventable Risks**: Olympus emphasizes that following the operation manual's **warnings, cautions, and inspection protocols** can help users identify and mitigate any risks associated with the reprocessor.
This recall not only urges end-user caution but also highlights the need for regular inspections and strict adherence to operational guidelines to ensure safety.
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### Details of the Recall
Here are the key details you need to know about the recall of the **OER-PRO Endoscope Reprocessor**:
- **Brand Name**: Olympus
- **Product Name**: OER-PRO Endoscope Reprocessor
- **Reason for Recall**: Olympus received notification of a fire-related incident involving the OER-PRO.
- **Safety Measures in Place**: Olympus urges all users to review and follow the warnings, precautions, and inspections outlined in the operation manual for the device.
- **Date Announced**: October 2023
- **Official Recall Notice**: [Visit the official recall notice here](https://recalls-rappels.canada.ca/en/alert-recall/oer-pro-endoscope-reprocessor).
If you’re a medical professional or facility using the Olympus OER-PRO, it’s crucial to act now to ensure safety and uninterrupted patient care.
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### What You Should Do
If your facility relies on the **OER-PRO Endoscope Reprocessor**, here’s a step-by-step guide to ensure compliance and safety:
- **Review Operational Manuals**: Carefully revisit all safety warnings, precautions, and inspection steps outlined in the OER-PRO’s manual.
- **Conduct Thorough Inspections**: Schedule immediate inspections of your device to identify any potential issues that could lead to safety risks, especially fire hazards.
- **Train Your Team**: Ensure your team is aware of the recall and understands how to operate the device safely and perform regular maintenance checks.
- **Report Issues**: If any malfunctions or concerns are identified, contact Olympus immediately for guidance or service options.
By acting promptly, healthcare providers can manage the situation effectively while maintaining safety for patients and staff.
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### Stay Safe – Get Instant Recall Alerts
To stay informed about potential safety risks and product recalls like this one, download our **Recall Alert App** today. With real-time notifications, detailed safety guidance, and an easy-to-navigate interface, you’ll always be the first to know about critical announcements in your industry.
Take charge of safety today — [download the app now](#) and safeguard your facility against preventable risks.
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For more information and the official recall notice, visit [the Canadian Recall database](https://recalls-rappels.canada.ca/en/alert-recall/oer-pro-endoscope-reprocessor). Stay proactive and keep your team and patients safe!