# Major Recall Alert: Octopus 4, Octopus Evo AS, and Octopus Nuvo Recalled Due to Misassembled Canister Tubing
On **January 7, 2026**, a critical recall was announced involving Medtronic's medical equipment, specifically the **Octopus 4**, **Octopus Evo AS**, and **Octopus Nuvo** products. During final inspection, it was discovered that the **canister tubing set had been misassembled**, causing a potential safety risk. The **short tube was mistakenly attached to the bottom of the canister**, while the **long tube was attached to the top**, which is **a reverse order from the design specification**.
This misassembly could impact the functionality of the product, raising concerns for patient safety and operational efficiency. Read on to learn more about the recall, why it matters, and how to take action if you are affected.
## Why This Recall is Important
Medical equipment plays a crucial role in healthcare, and even minor design flaws can lead to serious consequences. In this case, the **misassembled canister tubing set** may disrupt device operation during critical procedures, potentially compromising patient safety.
Medtronic, a trusted name in the medical industry, has issued this recall to prevent any adverse situations involving the impacted products. The **Octopus 4**, **Octopus Evo AS**, and **Octopus Nuvo** are commonly used devices in surgical settings, and proper functionality is essential for their intended applications.
If you or your healthcare facility uses these products, it’s important to review the recall details and take appropriate action immediately.
## Details of the Recall
Below are the key details of the January 2026 Medtronic recall:
- **Category**: Medical Device Recall
- **Products Affected**:
- **Octopus 4**
- **Octopus Evo AS**
- **Octopus Nuvo**
- **Issue Identified On**: January 7, 2026
- **Recall Reason**: Misassembled canister tubing set:
- The **short tube** was attached to the **bottom** of the canister.
- The **long tube** was attached to the **top**, which is **reverse** of the design specification.
- **Potential Risks**: Possible performance disruption that could compromise the device's intended use.
For more details, refer to the official announcement from Health Canada: [Click Here](https://recalls-rappels.canada.ca/en/alert-recall/octopus-nuvo-octopus-evo-and-octopus-4).
## What You Should Do
If you use or have distributed the affected **Octopus 4**, **Octopus Evo AS**, or **Octopus Nuvo** devices, follow these steps:
1. **Stop Using the Recalled Products**: Immediately discontinue use of the affected products in your facility or practice.
2. **Inspect Inventory**: Check your inventory for the recalled devices.
3. **Contact Medtronic**: Reach out to Medtronic’s customer service for further instructions on product return, replacement, or repair.
4. **Inform Key Stakeholders**: Notify relevant staff members and colleagues about the recall to ensure proper awareness and action.
Addressing this recall promptly is critical to ensuring patient safety and maintaining compliance with healthcare regulations.
## Stay Safe – Get Instant Recall Alerts
Staying informed about product recalls is vital for both healthcare professionals and patients. To ensure you never miss a critical recall update like this, consider downloading a reliable recall notification app.
- **Benefits of a Recall Alert App**:
- Real-time notifications about recalls in your industry.
- Easy access to detailed product information.
- Support for taking quick corrective action.
**Don’t leave safety to chance. Download a recall alert app today** to stay ahead and protect those who rely on you.
---
For more information about this recall, visit the official Health Canada recall page: [Octopus Nuvo, Octopus Evo AS, and Octopus 4 Recall Details](https://recalls-rappels.canada.ca/en/alert-recall/octopus-nuvo-octopus-evo-and-octopus-4).
Stay proactive, informed, and prepared. Always prioritize safety when using essential medical equipment.