# Major Recall Alert: Single Use Ligating Device PolyLoop™ Recalled Due to Malfunctioning Release in Patient Anatomy
Olympus has issued a crucial product recall for the **Single Use Ligating Device PolyLoop™**, following complaints about the device's inability to release or detach correctly during use. This defect can result in the loop becoming unintentionally anchored around patient anatomy, which poses risks to patient safety. If you or your medical team uses this product, it’s essential to be informed about this recall and take necessary precautions.
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## Why This Recall is Important
The **Single Use Ligating Device PolyLoop™** is a medical device commonly used in surgical procedures to ligate tissue safely. However, Olympus has acknowledged receiving several complaints indicating a key malfunction — the ligation loop does not release or detach as it should. If the loop becomes anchored in place unintentionally, it can lead to complications during the surgical procedure, including potential patient harm.
Understanding the gravity of these risks is vital for healthcare providers and facilities utilizing this device. Olympus has also emphasized the importance of adhering to the warnings and cautionary statements provided in the **Instructions for Use (IFU)** to mitigate risks during any procedures involving the affected devices.
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## Details of the Recall
Here’s what we know about the **Single Use Ligating Device PolyLoop™** recall:
- **Brand:** Single Use Ligating Device PolyLoop™
- **Category:** CAN (Canada)
- **Reason for Recall:** Complaints regarding the ligation loop failing to release or detach, causing it to unintentionally anchor in patient anatomy.
- **Safety Reminder:** Users are encouraged to follow all warnings and cautions detailed in the product's **Instructions for Use**.
- **Date Announced:** October 30, 2023
- **Image of Product:**
For the official recall advisory, visit the **[Government of Canada Recall Page](https://recalls-rappels.canada.ca/en/alert-recall/single-use-ligating-device-polylooptm)**.
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## What You Should Do
If you use or distribute the **Single Use Ligating Device PolyLoop™**, here’s how to proceed to ensure patient safety and compliance:
- **Check Your Inventory:** Immediately review all PolyLoop devices in your inventory to identify affected products.
- **Follow Guidelines:** Carefully adhere to the product's **Instructions for Use (IFU)**, particularly the safety warnings and cautions.
- **Contact Olympus:** Reach out to Olympus for additional guidance or to report any suspect devices.
- **Stop Use:** Discontinue the use of the affected devices and consider alternatives until the issue is resolved.
- **Notify Your Team:** Make sure all healthcare professionals in your organization are aware of the recall and directed to remove the product from use to prevent unintended complications.
Taking these steps promptly can help mitigate risks and ensure continued patient safety during procedures.
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## Stay Safe – Get Instant Recall Alerts
Ensuring patient safety and product compliance begins with staying informed. With the increasing number of medical product recalls, having real-time updates is critical.
**Download the My Recalls App** to:
- Receive **instant alerts** for product recalls in Canada and worldwide.
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Staying vigilant with medical device recalls like the **Single Use Ligating Device PolyLoop™** can protect patients and save lives. For more information on this recall, visit the **[official Government of Canada recall page.](https://recalls-rappels.canada.ca/en/alert-recall/single-use-ligating-device-polylooptm)** Stay informed, stay safe.