Immunoassay Blood Test For Amyloid Pathology Assessment

FDA product code SET · Class 2 · 7 devices · 0 reports · 7 devices named in recalls

• Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio CL0073

  Fujirebio Diagnostics, Inc. · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse G B-Amyloid 1-42-N Plasma 235447

  Fujirebio Inc. · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse G B-Amyloid 1-42-N Plasma Calibrator 235454

  Fujirebio Inc. · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse G pTau 217 Plasma Immunoreaction Cartridges 81550

  Fujirebio Europe · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse G pTau 217 Plasma Calibrators 81557

  Fujirebio Europe · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse pTau 217 Plasma Controls 81558

  Fujirebio Europe · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports
• Lumipulse B-Amyloid Plasma Controls 81559

  Fujirebio Europe · Immunoassay Blood Test For Amyloid Pathology Assessment
  1 recall0 reports