# Major Recall Alert: Allura Xper and Azurion Systems Recalled Due to X-Ray Imaging Issues with Wired Foot Switch
Philips has issued a critical recall affecting specific Allura Xper FD and Azurion imaging systems. The issue involves potential failures in X-ray imaging due to problems with the wired foot switch. This safety concern could lead to intermittent or failed imaging, with potentially significant consequences for medical procedures. Read on for important details about this recall and what steps you should take.
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## Why This Recall is Important
Medical imaging is critical for accurate diagnoses and effective treatment. The recall of select **Allura Xper and Azurion systems** highlights potential issues with the wired foot switch that could result in intermittent X-ray functionality or failure to initiate imaging altogether. This could cause:
- **Delays or interruption of medical procedures**
- Increased risk to patient safety during time-critical diagnoses or treatments
- Potential disruption of healthcare services
Understanding this recall is essential for healthcare facilities that rely on these advanced imaging systems.
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### Details of the Recall
Philips has identified several causes behind the X-ray imaging issues:
- **Cable or Connector Damage**: Internal or external damage to the wired foot switch cable or connector.
- **Internal Microswitch Failure**: Each pedal on the foot switch has two independent microswitches that work together to release X-ray. If one or both fail, functionality is compromised.
- **Connector Issues from Improper Strain Relief**: Missing or poorly applied strain relief can lead to connector failures.
#### Affected Products and Models:
The recall affects multiple models within the Allura Xper and Azurion product families, including:
- **Allura Xper Series**: FD10, FD10/10, FD20, FD20 Or Table, FD20/10, FD20/15, and FD20/20
- **Azurion Series**: 3 M12, 3 M15, 5 M12, 5 M20, 7 B12, 7 B20, 7 M12, 7 M20
For a complete list, visit the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-and-azurion-systems).
#### Recall Date:
The recall was officially announced on **October 15, 2023**.
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### What You Should Do
If your facility uses any of the affected systems, take the following steps immediately:
1. **Inspect Your Wired Foot Switch**
Look for signs of internal or external damage to the cable or connector.
2. **Check for Functionality**
Test the foot switch microswitches and connectors for proper operation.
3. **Contact Philips Support**
Notify Philips about your system. Philips will guide you through repairs, replacements, and any needed support to mitigate risks.
4. **Communicate Within**
Inform your staff about the recall and ensure everyone is aware of the issue to prevent delays during critical procedures.
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### Stay Safe – Get Instant Recall Alerts
Recalls like this underscore the importance of staying informed about product safety issues. To protect your patients and ensure smooth healthcare operations, download the **MyRecalls App** today. You'll receive **real-time alerts** for medical device recalls, helping you stay ahead of potential risks.
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Don't wait—get the app now and make recall management easier for you and your team.
Stay safe and informed by visiting the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-and-azurion-systems). Protect your patients and your practice by staying proactive.
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This recall serves as a critical reminder of the importance of regular equipment inspections, communication within healthcare teams, and prompt action when dealing with potential safety concerns. Stay informed, stay prepared, and prioritize patient safety at all times.