Reported Apr 8, 2026 · Ongoing
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
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 M20
- System Code
(1)722079(2)722224(3)722234(4)722282 (OUS only)
- Lot codes and dates
- (1)
- System Code722079
- UDI00884838085268
- System Serial Number
1,720 of 1,720 codes
10236456461013138746035404370330770390410481137401101010542665345355368184126172464885357905556919928098481033836891115546611571395703559263420703391673297298299564838103211179871310121112134713651408881
- System Code722224
- UDI00884838099258
- System Serial Number
2,837 of 2,837 codes
122945015761577157875040926126227227527729563010031315274435263819592321019137126010491484225830443045310725731083351433142184243624647518107623153526224158846996253942128890163527845023925205899115562945840
- System Code722234
- UDI00884838116771
- System Serial Number
522 of 522 codes
1633277803625022228033471618435228721232288716185426292432525960332973593463833008043407111869941354744933543781344735851051140448462621620724817587333395556865545971465
- System Code722282
- UDI00884838110571
- System Serial Number
91 of 91 codes
57546673327875536110111112451165981894247483126638399469139403484114434476289511513191011617517956301219741203377686598701188126
- Amount recalled
- 5167 units (1728 US, 3439 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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