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UHI-3 High Flow Insufflation System - Insufflator Recall Due to Olympus is in...

# Major Recall Alert: UHI-3 High Flow Insufflation System - Insufflator Recalled Due to Safety Concerns

Olympus has initiated an important **medical device recall** concerning several High Flow Insufflation Unit Models, including the **UHI, UHI-2, UHI-3, and UHI-E**. The affected devices, including the **UHI-3 High Flow Insufflation System - Insufflator**, pose potential safety risks. If you or your organization utilizes one of these devices, it is critical to **immediately stop usage** and **contact Olympus customer service** to arrange for the return of the product.

Please note that all affected models have been **discontinued for sale and repair**, making this recall an essential step in ensuring safety and compliance with regulatory standards.

Official Source: [UHI-3 High Flow Insufflation System Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/uhi-3-high-flow-insufflation-system-insufflator)

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## Why This Recall is Important

Medical devices, such as insufflators, play a critical role in various surgical and diagnostic procedures, delivering precise airflow to support patient care. However, when these devices present potential risks, they could compromise both patient safety and procedural accuracy.

The recall of the **UHI-3 High Flow Insufflation Unit** highlights Olympus’ commitment to addressing safety issues promptly, protecting both healthcare providers and patients alike. Whether you’re a hospital administrator, surgeon, or clinician, staying informed about this recall is vital.

Customers must be aware of the potential hazards that the affected units might pose and ensure they act quickly to mitigate any associated risks.

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## Details of the Recall

Olympus issued the recall for the following High Flow Insufflation Unit Models:

- **UHI**
- **UHI-2**
- **UHI-3 (High Flow Insufflation System - Insufflator)**
- **UHI-E**

### Key Points to Know:
- **Reason for Recall**: Olympus has determined that these devices may present certain risks to users and patients. No further sales, repairs, or replacements are being offered as these models are discontinued.
- **Action Required**: Customers are urged to **immediately stop usage** of any affected units.
- **Contact Information**: Reach out to Olympus customer service for instructions on returning the affected products.
- **Date Announced**: Official recall information was made available as of [Date: 31343].

For a visual reference:
![UHI-3 High Flow Insufflation System Image](https://myrecalls.app/images/products/31343_1770415529.jpg)

Official government listing here: [UHI-3 Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/uhi-3-high-flow-insufflation-system-insufflator).

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## What You Should Do

If your facility has been using any of the affected High Flow Insufflation Units, here are the steps you should take immediately:
1. **Stop Use Immediately**: Halt procedures involving the recalled products to prevent potential risks.
2. **Contact Olympus Customer Service**: Obtain instructions for returning your affected devices. Ensure you follow their guidance for safe handling and disposal.
3. **Check Inventory**: Audit your equipment inventory to identify any other impacted devices.
4. **Inform Staff**: Notify relevant personnel within your facility about the recall to avoid accidental usage.

Acting quickly can help minimize any risks to patient safety or disruption to surgical workflows.

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## Stay Safe – Get Instant Recall Alerts

The recall of the **UHI-3 High Flow Insufflation System - Insufflator** is just one of many important safety updates healthcare providers should be aware of. Ensuring your facility is always equipped with up-to-date recall information is critical.

Stay ahead of potential issues with **MyRecalls**, the recall tracking app! Download the app today to receive **instant alerts** on medical device recalls, product safety updates, and more. Be proactive in protecting your patients, colleagues, and organization.

👉 **Download the MyRecalls app now and stay informed!**

For additional details about this recall, visit the official government page: [UHI-3 High Flow Insufflation System Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/uhi-3-high-flow-insufflation-system-insufflator).

Stay safe, stay informed, and take action quickly to ensure compliance and safety in your practice.

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