Reported Feb 18, 2026 · Ongoing
Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X,…
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best, N/A · N/A
Is this the product you have?
- Azurion 7 M12 System Model Numbers
(1)722078(2)722223(3)722233
- Software Version Number - All versions
R1.XR2.XR3.X
- Lot codes and dates
- System Model Numbers
(1)722078(2)722223(3)722233
- UDI-DIs
(1)884838085251(2)884838099241(3)884838116764
- Serial NumbersAll
- System Model Numbers
- Amount recalled
- 1979 units (365 US, 1614 OUS)
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
- Nationwide
Why it was recalled
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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