Fujirebio Lumipulse pTau 217 Recall
Fujirebio's Lumipulse pTau 217 Plasma Controls (Model 81558) can produce inaccurate test results, potentially causing misclassification of Alzheimer's disease …
Fujirebio Diagnostics, Inc.
Fujirebio Diagnostics, Inc. Recalls (2026)
Every recall we are tracking for Fujirebio Diagnostics, Inc., newest first, sourced from the FDA. If you are wondering whether your Fujirebio Diagnostics, Inc. product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Fujirebio Diagnostics, Inc. recall posts.
1 recall · updated Dec 11, 2025
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Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
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Windstone Medical Packaging is recalling three AMS Aligned Medical Solutions medical convenience kits because the Lidocaine HCl injection included in them has …
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