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Medical Device

Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
Reason for recall
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Units affected
1523 units (322 US, 1201 OUS)
Description
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
View official recall notice →