# Major Recall Alert: Brilliance CT Big Bore System Recalled Due to Motion Issues in Interventional Control
Philips has initiated a significant recall of its **Brilliance CT Big Bore System - Main Unit, Brilliance CT Big Bore System - Software - Pulmonary Toolkit for Oncology, and Philips CT Big Bore** products. Two unintended motion issues related to interventional control have been identified, posing a potential **safety risk for operators and patients**. These issues may lead to collisions involving the gantry or table. This recall, which officially begins on **April 4, 2025**, is critical for ensuring the safety of healthcare professionals and patients.
Stay informed about this important recall and learn how you can take action to protect yourself and others.
## Why This Recall Is Important
Medical devices like the **Philips Brilliance CT Big Bore System** are widely used for diagnosing and treating critical health conditions, especially in oncology and interventional radiology. Any malfunction in these devices can lead to serious, unintended consequences, including physical harm to both patients and operators.
Philips has become aware of the following two **motion-related issues** in its interventional control systems:
- **Interventional control touch panel motion button not released:** This malfunction may cause the device to execute unintended movements, increasing the risk of collisions during procedures.
- **Plan box not updated during an interventional procedure:** When the plan box does not update as expected, it can lead to inaccurate or unsafe adjustments.
These issues underscore the importance of **regular maintenance, testing, and swift responses to recalls** to mitigate risks in medical environments.
## Details of the Recall
This recall affects the following products:
- **Brilliance CT Big Bore System - Main Unit**
- **Brilliance CT Big Bore System - Software - Pulmonary Toolkit for Oncology**
- **Philips CT Big Bore**
### Key Details:
- **Recall Reason:** Two unintended motion issues in the system’s interventional control
- **Risks:** Increased chances of a collision of the gantry or table with the operator or patient
- **Recall Start Date:** April 4, 2025
- **Brand Name:** Philips
Healthcare organizations currently using these systems are urged to assess whether their devices are affected and take immediate action to comply with Philips' recall process.
> For more information, you can access the official recall notice here: [Philips Brilliance CT Big Bore Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/philips-ct-big-bore).
## What You Should Do
If you are a healthcare professional or administrator responsible for the affected products, it is crucial to take the following steps:
- **Cease Use Immediately:** Stop using affected units to avoid potential collisions or inaccuracies during interventional procedures.
- **Consult the Recall Notice:** Refer to [Philips Brilliance CT Big Bore Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/philips-ct-big-bore) for detailed instructions and updates.
- **Contact Philips Support:** Follow official communication channels for replacements, repairs, or software updates to resolve the reported issues.
- **Inform Relevant Teams:** Communicate urgently with your team to ensure everyone is aware of the recall and safety protocols.
Patient safety and healthcare worker protection should remain a top priority when dealing with recalls of critical medical devices like this.
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Remember, timely awareness can prevent accidents and save lives. Stay ahead of important updates like the Philips CT Big Bore System recall to ensure the safety of everyone in your facility.