Reported Apr 8, 2026 · Ongoing
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
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 6 · Best · N/A
Is this the product you have?
- Azurion 7 B12
- System Code
(1)722067(2)722225(3)722235
- Lot codes and dates
- (1)
- System Code722067
- UDI00884838085350
- System Serial Number
202 of 202 codes
221421721731092501031929211422569214419881123278462771151501631317110413214720824475362341417026148133571281881516823311125543332214625627023818774154157251237222
- System Code722225
- UDI00884838099265
- System Serial Number
377 of 377 codes
1041534628722084112214737626233111211020737540440568177291299400291412162177137175205228229157340453532592603002685523529823335428914824943443540984111227455365284362468
- System Code722235
- UDI00884838116788
- System Serial Number
93 of 93 codes
77127768812431025971115557891374105118125135419470547247492139799327781420109108561063031142107103991371318283841001266667966334281718
- Amount recalled
- 670 units (106 US, 564 OUS)
This recall covers 23 products
The agency filed one notice per product. You are reading one of them; the other 22 are below.
10 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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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