# Major Recall Alert: Endoscope Reprocessor, OER-PRO Endoscope Reprocessor Recalled Due to Fire-Related Incident
Olympus recently announced an important safety notification involving its **Endoscope Reprocessor, OER-PRO Endoscope Reprocessor**. The company has reported a **fire-related incident** and is urging all users to carefully adhere to the **warnings, cautions, and inspection guidelines** provided in their endoscope reprocessor operation manuals. This recall is significant as these devices play a critical role in endoscope cleaning and disinfection processes in healthcare settings.
Healthcare facilities, technicians, and service providers using the **OER-PRO Endoscope Reprocessor** need to act immediately to prevent potential hazards and ensure patient and staff safety.
Read on to find out all essential details about this recall and how you can take action today.
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## Why This Recall is Important
This recall was made in response to a **fire-related incident**, which underscores the potential risks associated with improper use or overlooked inspections of the **OER-PRO Endoscope Reprocessor**. Endoscope reprocessors are essential in ensuring endoscopes are properly disinfected and safe for use on patients. A device malfunction or oversight could pose significant risks, including:
- **Fire hazards** that may lead to damage, injuries, or disruptions in healthcare environments.
- Potential operational downtime for healthcare providers.
- Compromised patient safety due to delays in critical procedures.
As a top leader in the healthcare technology space, Olympus issued this reminder to safeguard users while addressing issues promptly.
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## Details of the Recall
- **Category**: Endoscope Reprocessor
- **Brand**: Olympus
- **Product Name**: OER-PRO Endoscope Reprocessor
- **Recall Reason**: The recall follows a **fire-related incident involving the OER-PRO model**. Olympus has urged users to follow the detailed **warnings/cautions and inspections** in operation manuals to prevent similar occurrences.
- **Date Announced**: October 31, 2023
For additional information, users are encouraged to review the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/oer-pro-and-oer-elite-endoscope-reprocessor).
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## What You Should Do
If your healthcare facility uses the **OER-PRO Endoscope Reprocessor**, Olympus recommends the following immediate steps:
1. **Inspect the Device**: Carefully review your device for any signs of malfunction, wear, or improper operation.
2. **Follow Manufacturer Guidelines**: Revisit the operational manual for **warnings, cautions, and inspection procedures**, and strictly adhere to them.
3. **Report Incidents**: If you notice any concerns or experience issues, report them immediately to Olympus or the Canadian recall authority.
4. **Stay Updated**: Monitor official updates from Olympus and health authorities regarding further instructions or fixes.
Taking prompt action can minimize fire risks, device malfunctions, and operational downtimes.
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## Stay Safe – Get Instant Recall Alerts
Stay ahead of critical recalls that may impact patient safety, healthcare operations, and everyday lives. With more recalls and safety alerts announced monthly, staying informed can be challenging—but we can help.
**Download our free app today** to get **real-time recall notifications** directly to your phone. Don’t miss important product updates, safety measures, or warnings for the tools and devices you use every day.
### Take Action Now: Protect Your Facility and Patients
Click here to download the app and receive instant alerts on recalls like the **OER-PRO Endoscope Reprocessor**.
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For more information and the official recall notice, visit the **[Government of Canada recall page](https://recalls-rappels.canada.ca/en/alert-recall/oer-pro-and-oer-elite-endoscope-reprocessor).**
Stay informed. Stay prepared. Stay safe.