medical Class II Updated 2025-02-12

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (

Recalled Product

AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027

Hazard / Issue

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: (1) 722005 00884838059191(10) 00884838080805(10) (2) 722011 --- (3) 722027 00884838054196(21)
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