Reported Apr 8, 2026 · Ongoing
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
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 B20
- System Code
(1)722068(2)722226(3)722236
- Lot codes and dates
- (1)
- System Code722068
- UDI00884838085367
- System Serial Number
421 of 421 codes
5471784673351472051704554945644189544024722564149421533243233208589109407239505271443104370322136373442524308354752794001965101104467833073288285295406528329184350462304457
- System Code722226
- UDI00884838099272
- System Serial Number
861 of 861 codes
120122123124125126127153672092716751121052109111312113915810781145239105678114362758403702108545197380281688592593495319687921182183325690100272680724350891280270254107144761681691779
- System Code722236
- UDI00884838116788
- System Serial Number
243 of 243 codes
127371593452417251801502272351312882262312032620249121200208422053618381147148133313425419443158992140601185037832533539191280233481972216820451230382218632
- Amount recalled
- 1523 units (322 US, 1201 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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