Fujirebio Diagnostics recalls
Fujirebio Diagnostics appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2026-02-11.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Product Description: Lumipuls…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Version: Not Applicable P…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 Software Version: Not Applicable Product Description: Lum…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog Number: 81550 Software Version: Not Applicable Product De…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Product Description: Lumipul…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not Applicable Product Descrip…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Software Version: Not Applicable Product Descrip…
FDA Device · Class II · 2026-02-11 · Fujirebio Diagnostics