# Major Recall Alert: DuraDiagnost Recalled Due to Collimator Attachment Issue That May Pose Safety Risks
Philips, a trusted name in medical technology, has announced a recall for its **DuraDiagnost DXR systems** due to a potential safety hazard. Healthcare facilities utilizing these systems need to act promptly to ensure patient and user safety. The recall was announced on **March 12, 2025**, and applies to systems where the **collimator** may not be securely attached following repairs or replacements. This defect could result in the collimator falling off during operation, posing significant injury risks to patients and system users.
For complete details, visit the official recall notice: [Philips DuraDiagnost Recall Alert](https://recalls-rappels.canada.ca/en/alert-recall/duradiagnost-0).
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## Why This Recall is Important
Medical imaging systems like Philips DuraDiagnost play a vital role in diagnosing and treating patients. However, the discovery of a potential **collimator detachment issue** has raised concerns about their safe operation:
1. If the **collimator** (a critical component that shapes and sizes X-ray beams) is not correctly secured during repairs or replacements, it may pose hazards.
2. A **falling collimator** during operation can result in injuries to:
- Patients undergoing diagnostic imaging.
- Healthcare workers operating the system.
3. This issue could also disrupt medical imaging workflows, delaying diagnoses and treatments.
Repair quality and maintenance checks are essential, and this recall highlights the need for vigilance when operating critical imaging systems.
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## Details of the Recall
### Brand Involved:
- **Philips DuraDiagnost DXR Systems**
### Recall Reason:
- **Potential detachment of the collimator** if improperly secured during repair or replacement. This may cause the collimator to fall off during operation.
### Announcement Date:
- **March 12, 2025**
### Safety Concerns:
- Risk of **injuries to patients** and **healthcare professionals** due to equipment failure.
### Official Source:
Visit the [Government of Canada recall page](https://recalls-rappels.canada.ca/en/alert-recall/duradiagnost-0) for more information.
Philips and regulatory authorities are urging healthcare facilities using DuraDiagnost DXR systems to take immediate action by following the recommended safety measures.
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## What You Should Do
If your healthcare facility operates a Philips DuraDiagnost DXR system, follow these steps to mitigate risks:
1. **Check your system**: Identify if your DXR system's collimator has undergone recent repairs or replacements.
2. **Contact Philips**: Reach out to Philips customer support for detailed guidance and inspection protocols.
3. **Schedule Inspections**: Ensure all collimators are properly secured and tested to prevent potential detachment issues.
4. **Stay Informed**: Subscribe to updates regarding this recall on Philips' website or the Canada recall platform.
Failure to address this issue could result in both safety hazards and patient care disruptions.
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## Stay Safe – Get Instant Recall Alerts
Safety is paramount, especially when operating medical devices that are integral to patient care. Stay ahead by downloading our **free recall alert app**, which provides real-time notifications about recalls in Canada, ensuring you never miss critical updates.
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Healthcare providers and professionals must prioritize this recall to prevent injuries and ensure patient trust. For complete details, visit the official recall link: [Philips DuraDiagnost Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/duradiagnost-0).