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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Aesculap S4 Element 4.5mm Polyaxial Screws Orthopedic Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall Aesculap PEEK Intervertebral Body Fusion System Orthopedic Devices Aesculap, Inc. 2 United States USFDA
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5F7 Orthopedic Devices Aesculap, Inc. 2 United States USFDA
Excia Cemented Hip Stems Orthopedic Devices Aesculap Implant Systems 2 United States USFDA