# Major Recall Alert: Uroskop Omnia Recalled Due to Safety Risk Linked to Frequency Converter Overheating
A critical safety recall has been announced for the **Uroskop Omnia** due to an issue identified during proactive internal quality assurance checks. The problem stems from a defect in the frequency inverter's resistor, which, under rare and specific conditions, can overheat, potentially causing the plastic housing to catch fire. This recall is aimed at addressing potential risks to users and ensuring safety for all.
Keep reading to learn more about the recall details, safety measures, and what actions you should take.
## Why This Recall is Important
Safety risks associated with medical devices like the **Uroskop Omnia** are taken seriously to prevent harm to patients, practitioners, and facilities. This recall was initiated because of the potential overheating of a resistor in the frequency converter for the longitudinal table movement.
In rare circumstances, the following conditions could align to create a hazardous situation:
- An undetectable defect in the frequency inverter.
- Frequent activation of longitudinal table movement.
- Unfavorable installation-related factors.
If these factors occur simultaneously, the resistor may overheat, which could lead to the **plastic housing catching fire**. While the likelihood of this happening is low, the risk of fire represents a critical safety concern and serves as the driving force behind this recall.
## Details of the Recall
Below are the key details surrounding the **Uroskop Omnia** recall:
- **Brand Name**: Uroskop Omnia
- **Product Affected**: Uroskop Omnia devices equipped with the affected frequency inverter.
- **Reason for Recall**: Overheating of the frequency converter resistor under rare and specific conditions due to a defective relay combined with unfavorable installation-related factors.
- **Potential Risk**: Fire hazard due to overheating plastic housing.
- **Date Announced**: October 2023.
- **Recall Start Date**: June 17, 2025.
All healthcare providers and users of the Uroskop Omnia are urged to review this safety notice immediately.
## What You Should Do
If you or your facility uses the **Uroskop Omnia**, it’s essential to take the following steps:
1. **Stop Use Immediately**: Even though the risk is rare, discontinue use of the affected device to avoid potential hazards.
2. **Contact the Manufacturer**: Reach out to the appropriate distributor or manufacturer of Uroskop Omnia for guidance on next steps regarding replacement or repairs.
3. **Inspect Installation Conditions**: Check for any improper installation factors that may increase the risk of overheating.
4. **Follow Official Recommendations**: Refer to the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/uroskop-omnia) for ongoing updates and detailed safety instructions.
For further clarification, consult your facility’s maintenance team or medical device procurement specialist to ensure compliance.
## Stay Safe – Get Instant Recall Alerts
Medical device safety recalls like this one highlight the importance of staying up-to-date with the latest product updates and potential hazards. To ensure you never miss a recall that could impact your practice or personal safety:
**Download a Recall Alert App Today!** Stay informed with real-time notifications about recalls for medical devices, appliances, and consumer products. Protect yourself and your organization by acting quickly in response to safety alerts.
### Final Thoughts
The safety and wellbeing of healthcare providers and patients are paramount. While the likelihood of danger from the **Uroskop Omnia** is low, this recall is a preventative measure to eliminate all risks. If you own or use this product, take immediate action and follow the recall guidelines to ensure safety in your medical facilities.
Stay proactive, and don’t forget to visit the official recall notice for more information: [Uroskop Omnia Recall](https://recalls-rappels.canada.ca/en/alert-recall/uroskop-omnia).
By addressing recalls promptly, we contribute to creating safer medical environments for everyone.