# Major Recall Alert: Philips Allura and Azurion Systems Recalled Due to Potential Safety Risk with 1 Phase UPS Component
Philips has initiated a major recall for its Allura Xper and Azurion systems due to a safety risk involving the 1 Phase Uninterruptible Power Supply (UPS). This optional component is designed to support a controlled data-saving shutdown of the PC-based systems during power failures. However, Philips has identified critical issues that could lead to complete system failure, posing serious risks to patients during complex or urgent medical procedures.
**Recall Start Date:** July 31, 2025
**Affected Models:**
- Allura Xper FD10
- Allura Xper FD20
- Allura Xper FD20 OR Table
- Azurion 7 B12
- Azurion 7 B20
- Azurion 7 M12
- Azurion 7 M20
Healthcare providers and facilities using these systems are strongly encouraged to review this urgent recall announcement.
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## Why This Recall is Important
The recall stems from a critical safety concern with the 1 Phase UPS component, which is an integral part of these systems. The UPS is intended to provide temporary power to ensure that crucial data is saved before the system shuts down during a mains power failure. However, Philips has discovered that:
- The UPS may fail unexpectedly, causing a **complete loss of power.**
- Failures can occur without prior warning, even if main power is functioning.
- This issue could prevent the **system from starting up** or cause it to **shut down abruptly.**
For medical professionals relying on these systems to perform vital procedures, the consequences could be dire. Some medical procedures—such as treatment for acute ischemic stroke or ST-elevation myocardial ischemia—are highly time-sensitive. A system failure could result in delays, cancellation of treatment, and even life-threatening adverse health outcomes, including the risk of death.
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## Details of the Recall
Philips has officially recalled the following systems equipped with the 1 Phase UPS component:
- **Allura Models:** FD10, FD20, and FD20 OR Table
- **Azurion Models:** 7 B12, 7 B20, 7 M12, and 7 M20
### Key Recall Facts:
- **Component Affected:** 1 Phase Uninterruptible Power Supply (UPS)
- **Safety Concern:** Unanticipated component failure leading to complete system shutdown.
- **Potential Impact:** Delayed or canceled procedures, which could have life-threatening effects for critical patients.
- **Date Announced:** July 31, 2025
For more information, visit the official recall page here: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/allura-and-azurion-systems).
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## What You Should Do
If your facility uses any of the affected Allura or Azurion systems, take the following steps immediately:
1. **Identify Affected Devices:** Confirm whether your systems are equipped with the recalled 1 Phase UPS component.
2. **Monitor for Failures:** Stay alert for symptoms of system failure, such as an inability to start up or sudden shutdowns.
3. **Contact Philips:** Philips will provide guidance on potential repairs or replacement of the defective component.
4. **Implement Backup Plans:** Ensure you have contingency strategies in place to manage delays or failures during critical medical procedures.
Prompt action can help mitigate risks and ensure patient safety.
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## Stay Safe – Get Instant Recall Alerts
Patient safety and timely awareness of product recalls are paramount. To stay informed about critical medical device recalls like this one:
- **Download the Canadian Recall and Safety Alerts App:** Get real-time notifications about device recalls and safety alerts directly on your phone.
- **Visit the Official Source:** Stay updated with recall notices by visiting [Government of Canada Recall Notifications](https://recalls-rappels.canada.ca/en/alert-recall/allura-and-azurion-systems).
Protect your practice and your patients by staying informed. Don’t wait—take action today to address this urgent recall and maintain uninterrupted healthcare services.
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By staying up-to-date with recall notices, you can safeguard patient outcomes and handle equipment failures proactively. Be prepared—ensure that your facility follows the recommendations provided by Philips and reports any related issues promptly.