GORE VIABIL Biliary Endoprosthesis Recall
Some GORE VIABIL Short Wire Biliary Endoprosthesis devices were labeled with incorrect specifications. Devices marked as 10 mm diameter x 10 cm without drainage …
W L Gore & Associates, Inc.
Every recall we are tracking for W L Gore & Associates, Inc., newest first, sourced from the FDA. If you are wondering whether your W L Gore & Associates, 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 W L Gore & Associates, Inc. recall posts.
1 recall · updated May 22, 2026
Cardinal Health Presource surgical procedure kits containing MEDICOM Ritmed Neurological Sponges have been recalled due to unexpected variability in endotoxin …
Cardinal Health 200, LLC
Siemens Atellica CH Urine Albumin test kits may produce falsely low results for urea nitrogen and hemoglobin A1c levels, or experience delayed results due to …
Siemens Healthcare Diagnostics, Inc.
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2 contains an out-of-specification concentration of sodium azide. Lab technicians may …
Siemens Healthcare Diagnostics, Inc.
V-Loc 180 absorbable wound closure sutures (sterile medical devices) may have tears or holes in their sterile packaging, allowing contamination that can cause …
Covidien, LP
Windstone Medical Packaging is recalling three AMS Aligned Medical Solutions medical convenience kits because the Lidocaine HCl injection included in them has …
Windstone Medical Packaging, Inc.
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