# Major Recall Alert: Endoscopy Trocar, Endoscopy Trocar Reducing Converter Recalled Due to Visible Silicone Fragments
A critical recall has been issued for **Endoscopy Trocar** and **Endoscopy Trocar Reducing Converter** devices due to potential risks identified during investigations by **Aesculap AG**. The issue stems from the **yellow sealing component** of the affected **reusable trocar systems**, which exhibits **uneven edges with visible silicone fragments**, raising concerns about patient safety. If you or your organization uses these products, it’s essential to take immediate action to address this safety issue.
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## Why This Recall is Important
Patients and healthcare providers rely on the highest standards of quality and functionality during medical procedures, especially when using surgical tools like trocars. The **Endoscopy Trocar** recall highlights a critical flaw in the **yellow sealing component** of the devices. The **silicone fragments** can pose a significant risk during medical procedures, potentially leading to contamination or harm to the patient.
Failing to address this issue could result in severe medical complications, leaving healthcare practitioners vulnerable to serious outcomes. This recall emphasizes the need for vigilance and proactive measures to ensure patient safety and the use of reliable surgical instruments.
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## Details of the Recall
Here’s what you need to know about this recall:
- **Category:** CAN
- **Brand:** Endoscopy Trocar, Endoscopy Trocar Reducing Converter
- **Products Recalled:**
- **Endoscopy Trocar**
- **Endoscopy Trocar Reducing Converter**
- **Reason for Recall:**
Aesculap AG identified that the **yellow sealing component** on their **10mm and 12mm reusable trocar systems** has **uneven edges**, with visible silicone fragments potentially contaminating surgical sites.
- **Date Announced:** 30142
- **Image of Product:**
This issue underscores the importance of carefully inspecting any medical instruments, especially those included in this recall, before use in healthcare settings.
For more information about the recall, visit the official [Canadian recall website here](https://recalls-rappels.canada.ca/en/alert-recall/endoscopy-trocar).
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## What You Should Do
If you use or manage supplies that include the **Endoscopy Trocar (10mm or 12mm)** or **Endoscopy Trocar Reducing Converter**, take the following steps immediately:
- **Cease Use:** Stop using the affected devices until further guidance is provided.
- **Inspect Stock:** Check your inventory for the affected products detailed in the recall.
- **Contact the Manufacturer:** Reach out to **Aesculap AG** for further instructions or clarification regarding product returns or replacements.
- **Notify Your Healthcare Network:** Inform colleagues, surgical teams, and relevant departments to ensure they’re aware of the issue.
Prompt action can help mitigate risks and maintain the highest standard of patient care.
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## Stay Safe – Get Instant Recall Alerts
Staying informed about recalls like this one is paramount for maintaining the integrity of your medical practice or healthcare organization. To ensure you never miss an important recall alert:
**Download the MyRecalls app today!** Our app provides instant updates on product recalls in **Canada and beyond**, empowering you to keep your workplace and family safe from defective products.
**Act now to stay informed and protect your peace of mind.**
Access this and other essential recall information by downloading our app or visiting the official recall advisory at the [Government of Canada’s website here](https://recalls-rappels.canada.ca/en/alert-recall/endoscopy-trocar). Stay safe and stay prepared!