# Major Recall Alert: OES Pro Urology Resection Sheaths Recalled Due to Safety Concerns
Olympus has issued an urgent recall notice for its **OES Pro Urology Resection Sheaths**, specifically targeting the **cystoscope outer sheath, 22.5 Fr**. This **medical device recall**, which follows the previously issued FY25-022 recall of **October 2024**, requires users to immediately stop use of the affected products and follow return procedures. Here’s everything you need to know about this recall and how to proceed.
## Why This Recall Is Important
Medical device recalls are issued to address serious safety risks to patients and medical professionals alike. Olympus initiated this action as part of its commitment to ensuring the highest safety and quality standards for its products.
The **cystoscope outer sheath, 22.5 Fr**, is a critical component used during urological medical procedures, such as resection and diagnostic interventions. However, the identified issues with this product may pose a risk of harm, emphasizing the importance of responding promptly to Olympus’s recommendations. Ensuring that all affected items are removed from use is crucial to patient safety.
## Details of the Recall
Here’s a breakdown of the key details regarding this voluntary recall:
- **Category**: Medical device
- **Product Name**: OES Pro Urology Resection Sheaths
- **Affected Component**: Cystoscope outer sheath, 22.5 Fr
- **Reason for Recall**: Following the October 2024 FY25-022 notice, Olympus flagged additional concerns with this component. Users are instructed to immediately stop usage due to potential risks.
- **Date Announced**: October 2024
Officials are asking affected users to immediately cease use of any **cystoscope outer sheath, 22.5 Fr** within their inventory. Olympus will be working closely with healthcare providers and distributors to ensure all impacted products are retrieved efficiently.
An **official source for this recall** with further updates can be found [here](https://recalls-rappels.canada.ca/en/alert-recall/oes-pro-urology-resection-sheaths-0).
## What You Should Do
If you have the affected **OES Pro Urology Resection Sheaths** in your inventory, here are the next steps to take:
- **Stop Usage Immediately**: Do not use the 22.5 Fr cystoscope outer sheaths for any medical procedures.
- **Contact Olympus Customer Service**: Provide details of any affected product in your possession. Olympus will assist with issuing a **Return Material Authorization (RMA)** for affected devices.
- **Follow Return Instructions**: Ensure the product is returned in line with Olympus’s guidelines to avoid any risks or delays in the recall process.
- **Monitor Updates**: Stay informed through official recall channels and your Olympus point of contact for additional updates as the recall progresses.
Healthcare professionals are strongly encouraged to report any incidents or adverse events related to this product to the appropriate regulatory authorities.
## Stay Safe – Get Instant Recall Alerts
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### Final Thoughts
Recalls like this one from Olympus underscore the importance of vigilance and prompt action when safety concerns arise. If you use or distribute **OES Pro Urology Resection Sheaths**, act now to comply with the recall directive. For further details, please consult the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/oes-pro-urology-resection-sheaths-0).
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