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Medical Device

Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
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
920 units (168 US, 752 OUS)
Description
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
View official recall notice →