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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
Recalled September 20, 2023 · FDA recall Z-2587-2023 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V
Hazard
A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible. · FDA Class II
Units
19,115 systems
Sold at
Worldwide distribution
Description
A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.
Product
Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
Manufacturer(s)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →