# Major Recall Alert: Olympus ViziShot 2 Flex Devices Recalled Due to Patient Safety Concerns
On **August 13, 2025**, Olympus announced a major medical device recall for its **ViziShot 2 Flex (19g)** devices due to concerns over **potential patient safety issues**. All healthcare providers and users are urged to immediately stop using the affected devices and return them as outlined in the **medical device recall letter**. Olympus is also addressing this issue by reinforcing key warnings in their **Instructions for Use (IFU)** to promote safer handling of these products.
If you're a medical professional or distributor, continue reading to learn more about the recall and the steps you must take to ensure patient safety.
## Why This Recall is Important
Medical device recalls must always be taken seriously, as they directly impact patient safety and care quality. The **ViziShot 2 Flex (19g)** device is designed for use in medical settings, but Olympus has identified a potential safety issue that could compromise its effectiveness or pose risks during procedures.
The recall not only addresses the immediate issue by removing affected devices but also highlights the importance of strict adherence to **updated safety guidelines** outlined in the IFU. Failing to act promptly could lead to risks that could have otherwise been prevented.
Ensuring all recalled devices are identified, returned, and replaced is crucial to maintaining high standards in patient care and medical facility safety.
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## Details of the Recall
Here’s what you need to know about the Olympus **ViziShot 2 Flex (19g)** recall:
- **Brand**: ViziShot 2 Flex
- **Product**: ViziShot 2 Flex (19g) medical device
- **Recall Reason**: Potential patient safety issues identified by Olympus
- **Recall Start Date**: August 13, 2025
- **Date Announced**: August 13, 2025
- **Action Required**:
- **Stop using** any affected devices listed in the official recall letter.
- **Return affected devices** to Olympus.
- **Further Safety Measures**: Olympus is reinforcing the **Instructions for Use (IFU)** to highlight safety precautions.
For more details on this recall, visit the official recall notice from the Government of Canada: [**ViziShot 2 Flex Recall Notice**](https://recalls-rappels.canada.ca/en/alert-recall/vizishot-2-flex).
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## What You Should Do
It’s essential to take swift action if you or your organization is impacted by this recall. Follow these steps to ensure compliance:
1. **Identify Affected Products**: Review the devices listed in the medical device recall letter from Olympus.
2. **Immediately Stop Usage**: Do not use any product identified in the recall, as continued use could pose patient safety risks.
3. **Return Products to Olympus**: Follow instructions provided in the recall letter to return any affected products directly to the manufacturer.
4. **Review Updated IFU**: Ensure medical professionals handling ViziShot 2 Flex devices are familiar with Olympus’ updated Instructions for Use (IFU).
Acting quickly helps maintain both patient safety and professional integrity within your healthcare practice.
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## Stay Safe – Get Instant Recall Alerts
With frequent product recalls and safety updates in the medical field, staying informed is more critical than ever. You can keep yourself and your organization safe by subscribing to instant recall alerts via trusted platforms.
**Stay One Step Ahead: Download the Recall App Today!**
Our app provides real-time updates on recalls, including medical devices like the **ViziShot 2 Flex**. By staying informed, you can quickly address safety risks, prevent incidents, and protect your patients or clients.
[**Download the Recall App Now!**](#)
For further details on this recall, visit the official recall page here: [ViziShot 2 Flex Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/vizishot-2-flex).
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### Final Thoughts
The **Olympus ViziShot 2 Flex (19g)** recall serves as a reminder of the importance of vigilance when it comes to medical device safety. If you or your organization uses this device, take immediate action by following the recall instructions provided.
Remember, staying informed is the best line of defense against safety risks. Download the Recall App, monitor updates, and prioritize the safety of those in your care.