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  • Dispositivo 988
  • Fabricante 214
  • Evento 124969
  • Implante 233
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall smith & nephew Orthopedic Devices Smith & Nephew, Inc., Endoscopy Div. 1 United States USFDA
Device Recall Smith & Nephew Orthopedic Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith and Nephew TWINFIX QUICKT Orthopedic Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew Dyonics Saw Blade General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew Dyonics Saw Blade General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew Dyonics Saw Blade General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10 General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 12 General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 14 General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16 General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 3 INCH General and Plastic Surgery Devices Smith & Nephew, Inc. 1 United States USFDA
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.