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 Table System
- Model numbers
- System Model Numbers: (1)722068, (2)722226, (3)722236, UDI-DIs: (1)884838085367, (2)884838099272, (3)884838116801, 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 B20 System is a medical imaging table used in various diagnostic and surgical settings. It is designed to support patients during procedures requiring imaging technology.
Why This Is Dangerous
The defect allows the table to move unpredictably, even with a lock engaged, which can jeopardize patient safety during procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall poses a significant safety risk to patients and healthcare providers, necessitating immediate action to prevent injuries.
Practical Guidance
How to identify if yours is affected
- Check if your model number is 722068, 722226, or 722236.
- Verify the software version number is R1.X, R2.X, or R3.X.
- Contact Philips Medical Systems for confirmation if unsure.
Where to find product info
Model numbers are typically located on the device's identification label, usually found on the back or bottom of the table.
What timeline to expect
Expect a refund or replacement processing timeline of 4-6 weeks after the recall is acknowledged.
If the manufacturer is unresponsive
- Document all correspondence with Philips Medical Systems.
- Follow up with a phone call if you do not receive a response within a week.
- Consider filing a complaint with the CPSC if no resolution is found.
How to prevent similar issues
- When purchasing medical devices, ensure they have reliable safety certifications.
- Check for recent recalls on similar medical devices before purchase.
- Stay informed about product safety updates from manufacturers.
Documentation advice
Keep a record of all communications regarding the recall, including emails, call logs, and any response from Philips Medical Systems.
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Product Details
The recalled models include Azurion 7 B20 System Model Numbers: 722068, 722226, and 722236. They were distributed worldwide, with 326 units in the U.S. and 1,177 units internationally. The devices have all software version numbers: R1.X, R2.X, R3.X.
Key Facts
- Recall Date: January 26, 2026
- Report Date: February 18, 2026
- Quantity Recalled: 1,503 units
- Hazard: Table may move unexpectedly
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Safety Guide
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