PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

Recall date

March 3, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1677-2026

FDA classification

Class II

Brand / firm

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Sold / distributed

Domestic: Nationwide Distribution; International: Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Botswana, Brazil, Brunei Darussal, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colo…

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;