Fujirebio Diagnostics, Inc. recalls

7 recalls on record · latest: December 11, 2025

Official U.S. recall history for Fujirebio Diagnostics, Inc., compiled from official government records.

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Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog Number: 81550 Software Version: Not A…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Software Version: Not Applic…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Versi…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Product…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not Applic…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 Software Version: Not Applicable Prod…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…

Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Product D…

December 11, 2025 · Medical device recalls Moderate risk Customers may experience inaccurate test results by observing a higher frequenc…