medical Class II Updated 2025-02-12

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 72

Recalled Product

Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280

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) 722064 00884838085282(21); (2) 722222 00884838099210(21); (3) 722280 00884838103276(21)
View official government recall

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