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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1301-2026
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Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Softwar... 2 02/05/2026 FEI # 2521625
Fujirebio Diagnostics, Inc.
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