Medical DeviceView official recall notice →
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Brand / Firm
Product
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
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
298 units (27 US, 271 OUS)
Description
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;