Quick Facts at a Glance
- Recall Date
- January 26, 2026
- Hazard Level
- HIGH
- Brand
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Product type
- Medical Imaging System
- Model numbers
- System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only), UDI-DIs: (1)884838085268, (2)884838099258, (3)884838116771, (4)N/A +1 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 26, 2026
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. or your healthcare provider for instructions. Notification method: N/A
About This Product
The Azurion 7 M20 system is a medical imaging device used in various healthcare settings. It assists in diagnostic procedures and treatments, making it essential for many medical professionals.
Why This Is Dangerous
The hazard occurs when the Reset Geometry button is pressed, causing the table to move unexpectedly even if a lock is engaged. This malfunction can endanger patients and staff during medical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects healthcare facilities using this system, requiring immediate action to ensure patient safety and avoid potential injuries.
Practical Guidance
How to identify if yours is affected
- Locate the model number on your Azurion 7 M20 device.
- Confirm if the model number matches any of the recalled models: 722079, 722224, 722234, or 722282 (OUS only).
- Check the software version against R1.X, R2.X, or R3.X.
Where to find product info
Model and serial numbers can typically be found on a label affixed to the device or in the user manual.
What timeline to expect
Expect a timeline of 4-6 weeks for the refund or replacement process from the manufacturer once all documents are submitted.
If the manufacturer is unresponsive
- Contact Philips Medical Systems again using alternative communication methods.
- Reach out to your healthcare provider for assistance.
- File a complaint with the relevant health authorities if necessary.
How to prevent similar issues
- Ensure that any future medical devices have up-to-date safety certifications.
- Look for devices with strong customer reviews regarding safety and reliability.
- Consult with healthcare professionals about the latest safety standards in medical equipment.
Documentation advice
Document all communications related to the recall, including emails and phone calls, and keep copies of any receipts or purchase confirmations.
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Product Details
The recall involves Azurion 7 M20 system models 722079, 722224, 722234, and 722282 (OUS only). These units were distributed worldwide, including 1,743 in the US and 3,393 in other countries. They were sold at various medical equipment suppliers.
Key Facts
- Recall date: January 26, 2026
- Report date: February 18, 2026
- Quantity recalled: 5,136 units
- Distribution: Worldwide, including the US and multiple countries
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Safety Guide
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