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)722078, (2)722223, (3)722233, UDI-DIs: (1)884838085251, (2)884838099241, (3)884838116764, Serial Numbers: All
- 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 M12 System is a medical imaging device used in healthcare settings for various procedures. It is designed to assist healthcare providers in performing imaging diagnostics effectively.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
This recall affects healthcare providers and patients who rely on the Azurion 7 M12 System for medical imaging. The unexpected movement can lead to procedural complications and potential injuries.
Practical Guidance
How to identify if yours is affected
- Check if your device model number is 722078, 722223, or 722233.
- Verify if your software version is R1.X, R2.X, or R3.X.
- Contact Philips Medical Systems if you are uncertain about the recall status.
Where to find product info
Locate the model number and software version on the device's label or user manual.
What timeline to expect
Expect a response from Philips Medical Systems regarding refunds or replacements within 4-6 weeks.
If the manufacturer is unresponsive
- Follow up with Philips Medical Systems via phone or email.
- Contact the FDA for guidance on reporting unresponsive manufacturers.
How to prevent similar issues
- Inquire about the latest models with updated safety features when purchasing medical imaging systems.
- Ensure that the device has undergone recent safety evaluations before use.
- Look for certifications by relevant health authorities.
Documentation advice
Keep records of your device’s details, including model number and software version, as well as any correspondence with the manufacturer.
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Product Details
The recall affects Azurion 7 M12 System models 722078, 722223, and 722233. All software versions R1.X, R2.X, and R3.X are included. The systems were distributed worldwide, with 365 units in the U.S. and 1,614 units internationally.
Key Facts
- Recall date: January 26, 2026
- Software versions: R1.X, R2.X, R3.X
- Total units recalled: 1,979
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Safety Guide
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