# Major Recall Alert: SIGNA™ Explorer Recalled Due to Scan Resumption Issue Beyond Safe SAR Limits
GE Healthcare has issued an important recall for its SIGNA™ Explorer MR systems due to a potential safety risk involving the scanning process. The recall, announced on February 12, 2025, addresses an issue where scans can be resumed even when the "6-minute average SAR" (Specific Absorption Rate) exceeds the limit displayed on the SAR monitor. This discrepancy poses a potential risk for overheating during magnetic resonance imaging (MRI) scans, making this recall critical for healthcare providers and patients alike.
For more details, you can access the official recall notice here: [SIGNA™ Explorer Recall Information](https://recalls-rappels.canada.ca/en/alert-recall/signatm-explorer).
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## Why This Recall is Important
Ensuring the safety of medical imaging devices is essential in healthcare settings. The SAR parameter determines how much radiofrequency energy is absorbed by a patient’s body during an MRI scan. Exceeding the "6-minute average SAR" threshold could lead to thermal injuries or adverse effects, especially during prolonged imaging procedures.
The issue identified with SIGNA™ Explorer’s power monitoring system allows scans to resume despite exceeding SAR safety limits—a situation that could compromise patient safety. For this reason, GE Healthcare is taking proactive steps to alert healthcare providers and address the problem.
If your facility uses SIGNA™ Explorer MR systems, be sure to review the recall details and implement the recommended actions to minimize any potential risks.
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## Details of the Recall
Below are the key details regarding this recall:
- **Brand and Product**: SIGNA™ Explorer by GE Healthcare
- **Recall Start Date**: February 12, 2025
- **Reason for Recall**: Scans can resume following a power monitor trip even when the "6-minute average SAR" exceeds the indicated limit.
- **Category**: Magnetic Resonance (MR) Systems
- **Safety Concern**: Potential thermal injuries caused by exceeding SAR safety thresholds.
- **Issued By**: GE Healthcare in coordination with safety regulators.
This recall is targeted specifically at healthcare facilities that utilize SIGNA™ Explorer MR systems to ensure compliance with SAR safety guidelines.
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## What You Should Do
If your facility owns or operates a SIGNA™ Explorer MR system, it’s crucial to act immediately to ensure patient safety and regulatory compliance. Here are the steps you should take:
- **Cease Use for Affected Systems**: Stop using SIGNA™ Explorer MR systems that may be impacted by the recall.
- **Contact GE Healthcare**: Reach out to GE Healthcare for further instructions on software updates or corrective measures.
- **Report Any Incidents**: Notify GE Healthcare and relevant authorities if any SAR-related issues occur.
- **Follow Official Guidance**: Refer to the official [recall notice](https://recalls-rappels.canada.ca/en/alert-recall/signatm-explorer) for updated information and follow the safety measures advised.
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## Stay Safe – Get Instant Recall Alerts
Patient safety is non-negotiable, and staying informed is the first step toward ensuring that the medical devices you rely on meet the highest quality standards. For real-time updates on safety recalls, regulatory alerts, and important healthcare news, download our **Recall Alerts App** today.
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This recall serves as a reminder of the importance of vigilance and proactive measures in maintaining patient safety in healthcare. If you operate SIGNA™ Explorer systems, don’t delay in addressing this issue. For complete details on the recall by GE Healthcare, visit [Canada’s Official Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/signatm-explorer).