# Major Recall Alert: Single Use Electrosurgical Snare SD-400 Recalled Due to Sterility Concerns
Olympus Medical has issued a significant recall for its Single Use Electrosurgical Snare SD-400. The investigation revealed that small holes might develop during packaging or transportation, potentially compromising the sterility of the device. Impacted lots (27V - 57V) must not be used due to the risk of contamination. Read on to learn why this recall is critical and what steps you need to take to ensure the safety and effectiveness of medical operations.
## Why This Recall is Important
Medical devices must meet strict safety and sterility standards to ensure optimal patient outcomes. Olympus’s Single Use Electrosurgical Snare SD-400 is a critical tool used in various surgical procedures, and any sterility breach could lead to severe health complications, including:
- **Infections** from non-sterilized medical devices.
- **Extended recovery times** for patients exposed to contaminated tools.
- **Potential legal and compliance issues** for healthcare institutions using the recalled lot numbers.
Recognizing these risks, Olympus is urging healthcare professionals to cease the use of affected products immediately. The integrity of medical devices is non-negotiable, especially when patient safety is at stake.
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## Details of the Recall
Here’s everything you need to know about this important recall:
- **Brand/Manufacturer**: Olympus Medical
- **Product Name**: Single Use Electrosurgical Snare SD-400
- **Reason for Recall**:
- Small holes may occur during packaging and transportation.
- Such holes create a **sterility breach**, making the device unsafe for use.
- **Impacted Lots**: 27V through 57V (inclusive).
- **Date Announced**: October 2023
- **Official Source**: [See Full Recall Notice Here](https://recalls-rappels.canada.ca/en/alert-recall/olympus-medical-single-use-electrosurgical-snare-sd-400).
This issue underlines the importance of rigorous manufacturing and transportation protocols for medical equipment. Olympus is working to resolve this problem and has urged healthcare providers to take immediate action.
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## What You Should Do
If you or your institution is using the affected Olympus Single Use Electrosurgical Snare SD-400, it’s crucial to follow these steps to safeguard patients and comply with recall procedures:
1. **Stop Using Recalled Lots**: Immediately identify and separate the impacted lot numbers (27V - 57V) from your inventory.
2. **Report the Issue**: Contact Olympus Medical to report usage of the affected products and coordinate their return or replacement.
3. **Follow Healthcare Protocols**: Report the recall to your institution’s risk management team to review safety protocols for patient care.
4. **Spread Awareness**: Inform your colleagues and professional networks about this recall to prevent accidental use of the defective lots.
Failure to take these steps could result in compromised patient safety and regulatory compliance risks.
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## Stay Safe – Get Instant Recall Alerts
Staying informed is the key to ensuring the safety of your patients, staff, and practice. With recurring product recalls like this one, being proactive about recall news has never been more critical.
Download the MyRecalls app today and receive instant alerts about product recalls that impact your industry. Our app ensures you never miss an important notice, whether it’s for medical devices, food, or consumer goods.
Click here to [download the MyRecalls app](https://myrecalls.app) and stay ahead of potential hazards.
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For more information on this recall, visit the official [Government of Canada Recalls Website](https://recalls-rappels.canada.ca/en/alert-recall/olympus-medical-single-use-electrosurgical-snare-sd-400). Stay informed, stay safe, and take immediate action on such recalls to prevent harm and reduce risks in critical healthcare environments.