medical Class II Updated 2025-02-12

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3

Recalled Product

Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281

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) 722228 00884838099234(21); (2) 722232 00884838116757(21); (3) 722281 00884838110564(21)
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