State
72,820 recalls have nationwide distribution and so reach Tennessee. 7,818 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,818 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,652 (21%) are Severe.
Which agencies issued them
These figures cover only the 7,818 recalls whose distribution notice names Tennessee specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Deli Jerry fuel containers sold on Walmart.com are recalled because their caps are not child-resistant, posing burn and poisoning risks to children. No injuries have been reported; consumers should stop using them and contact Deli OfficeSupplies for a refund.
SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.
Hampton Bay Halwin 52-inch ceiling fans are being recalled because the fan blades can separate from the motor flywheel, posing impact and injury risks. About 9,460 units sold at Home Depot between January 2023 and October 2025 are affected.
Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.
Chrysler is recalling 81 2026 Jeep Grand Cherokee and Grand Cherokee L vehicles because a software issue may cause windshield wipers to fail, reducing visibility.
DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.
AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.
Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.
AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.
Nissan is recalling 2025 Altima vehicles because incorrect mounting fasteners may prevent front passenger air bags from deploying as intended in a crash.
OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.
Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.
AVID Medical, Inc. is recalling 5,168 Halyard convenience kits because they contain Medline Namic Angiographic Star Off Handle Manifolds that may have particulates in the fluid path.
Zydus Pharmaceuticals is recalling Mirabegron extended-release tablets, 25 mg, due to an out-of-specification result for the N-Nitroso Mirabegron impurity. The recall affects nationwide distribution in the USA.
Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.
Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.
BMW is recalling certain 2024-2026 X3 models because the steering spindle may be incorrectly attached to the steering column, increasing crash risks.
AKKARCO LLC is voluntarily recalling Ashfiat Alharamain Energy Support (250ml/8fl. oz.) because it contains undeclared tadalafil.
Pride Mobility is recalling 1,102 Quantum Rehab 4Front powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.
Cyclophosphamide for Injection, USP, 2 gram/vial, is being recalled due to the presence of particulate matter identified as stainless steel. The recall affects 1,464 vials distributed nationwide.
United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.
Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.
Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.
Beckman Coulter is recalling MicroScan LabPro V5.03 Panel Update 11 DVD Kits due to incorrect algorithms that may affect antimicrobial susceptibility test results, potentially leading to false susceptibility classifications.
Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.