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.
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
ChloraPrep FREPP sterile skin antiseptic applicators were distributed without proper sterilization, posing a risk of infection. These applicators are used …
CareFusion 213, LLC
ConvaTec is recalling Aquacel Ag Surgical SP surgical dressings (REF 413556, 9cm x 15cm size) because some were made thicker than the design specification. The …
ConvaTec, Inc

SUNS International is recalling SS6291 Solenoid Interlock Switches used in residential elevators because the switch can get stuck in a retracted position, …
SUNS SS6291 Solenoid Interlock Switches
Remel GC Agar Base laboratory media may not properly recover some strains of Neisseria gonorrhoeae bacteria, potentially leading to missed or delayed diagnoses …
Remel, Inc
Medline Convenience kits containing Swan-Ganz catheters are being recalled due to failures in the blue proximal injectate lumen hub that can leak or break, …
Medline Industries, LP
Medline Convenience kits containing Swan-Ganz catheters are being recalled because the blue proximal injectate lumen hub can leak, break, or fail, risking …
Medline Industries, LP
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