State
73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Steris Corporation is recalling VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false-negative steam sterilization results.
Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results.
K.C. Pharmaceuticals is recalling Leader Advanced Relief Eye Drops and related brands due to a lack of assurance of sterility. The recall covers 208,896 cartons distributed nationwide.
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.
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.
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
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.
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.
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.