PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C System Code: (1) 722001
Recalled Product
Allura Xper FD10C System Code: (1) 722001
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
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