Reported Apr 8, 2026 · Ongoing
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
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 M12
- System Code
(1)722078(2)722223(3)722233
- Lot codes and dates
- (1)
- System Code722078
- UDI00884838085251
- System Serial Number
779 of 779 codes
302585410753523293840291536537870613598679224829249546478479513278437438456566833488327550571544545465376319217001654455396546566576584361007862786308396576121239383491125500645379
- System Code722223
- UDI00884838099241
- System Serial Number
1,034 of 1,034 codes
31232433258585533189479103847114635239132868110521130388581855905570774484955711711051439126628361088580117912411065799577106011071114323252626261207329100180156056120537944020419219717737
- System Code722233
- UDI00884838116764
- System Serial Number
183 of 183 codes
6412216917026796144212153259118214415912414710310811117212719221821925012337381832733041713776300122012388228829529729881412627235681413813911727958240287280281
- Amount recalled
- 1994 units (360 US, 1634 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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