Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Apothecary Pharma is recalling NAD+ Injection vials due to a lack of assurance of sterility. The product was distributed nationwide.
Canon Medical System is recalling one Alphenix INFX-8000C/B5 unit in Idaho due to a risk of tabletop shifting that could cause patient misalignment.
Toyota is recalling 2024-2027 Land Cruiser Hybrid vehicles because a fuel tube connection may disconnect and leak fuel, increasing fire risk.
The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts due to undeclared milk. The product was distributed nationwide.
Sweet Sensi is recalling Passion Guava Kush THC gum drops nationwide due to the detection of Staphylococcus aureus.
Steris Corporation is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low to accurately monitor steam sterilization cycles.
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 76/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
K.C. Pharmaceuticals is recalling multiple brands of eye drops due to a lack of assurance of sterility. The recall covers 1,435,830 cartons distributed nationwide.
GIAS Food Inc. is recalling 1,174 cases of Lemon Alfredo Fettuccine due to contamination with Listeria monocytogenes. The product was distributed to retail locations nationwide.
Cardinal Health 200, LLC is recalling 210 Presource Packs containing Medtronic Microstream components due to reports of difficulty disconnecting the adapter, which can cause treatment delays or unintended extubation.
Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Saint Francis Apizza LLC is recalling 1,920 units of Frozen Supreme Pizza due to undeclared soybean oil and soy lecithin. The product was distributed in Kentucky and Ohio.
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Queso Palmita GP LLC is recalling 20 packages of frozen Pastel de Queso (Cheese Pie) in Texas due to undeclared milk.
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
Saint Francis Apizza LLC is recalling 4,255 units of frozen cheese pizza due to undeclared soy ingredients. The product was distributed in Kentucky and Ohio.
Saint Francis Apizza LLC is recalling 2,655 units of frozen Mushroom & Onion Pizza in Kentucky and Ohio due to undeclared soy ingredients.
J K Patisserie & Bakery LLC is recalling croissants because egg was not declared in the Contains statement. The product was distributed in New York and New Jersey.
J K Patisserie & Bakery LLC is recalling 87 units of Lemon Blueberry Loaf because the product contains undeclared soybean oil and soy lecithin.
Saint Francis Apizza LLC is recalling 4,931 units of frozen pepperoni pizza due to undeclared soybean oil and soy lecithin.
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.