State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 35,300 Magellan Odyssey Rocker Chairs sold by Academy Sports + Outdoors are being recalled because the chairs' legs can break.
About 1,500,000 Angry Orange Enzyme Stain Removers are being recalled in the US because they can contain bacteria including Pseudomonas aeruginosa.
About 340 Gagaku ice cream shop toy playsets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.
About 29,000 Iristar Minoxidil Spray Bottles are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 47,000 Matrix and Vision treadmills are being recalled because the power cord can become loose from the power socket, posing a fire hazard.
Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.
Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.
Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.
Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.
Oshkosh is recalling 230 2025 NGDV and NGDV Electric vehicles because rear axle hub fasteners may loosen, potentially causing the wheel to detach.
Ford is recalling 2026 Explorer vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the high voltage battery cell modules may contain misaligned electrodes that can result in a battery fire.
Gold Star Distribution is recalling Halls Cough Drops across multiple flavours over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Hologic is recalling 3,728 units of ThinPrep CytoLyt Solution over fungal contamination of the affected lot with Parengyodontium album.
Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Liquid NyQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Boston Scientific is recalling 21 Coyote over-the-wire PTA balloon dilatation catheters over the potential for inflation and deflation difficulty during use in the peripheral vasculature.
Gusto Group is recalling 7 cases of Klong Kone shrimp paste after the product tested high for lead.
Medtronic is recalling 442 Abre Venous Self-Expanding Stent Systems because a nitinol anomaly causes a reduced stent diameter and radial force when deployed, which may result in migration.
Intuitive Surgical is recalling 41,526 da Vinci SP Access Port Kits because the Access Port System tray may develop cracks, potentially resulting in a sterility breach.
Eureka Inc is recalling 32 cases of ground cinnamon in 100g clear plastic containers over elevated levels of lead.
ICU Medical is recalling 423 Plum Duo Infusion Systems after one lot of defective primary speakers may fail to produce sound, so the pump may not produce audible alarms or alerts.
Ford is recalling 2025 F-59 and F-53 vehicles because an incorrectly installed switch may cause brake lights to malfunction, increasing crash risk.
Elekta is recalling a MOSAIQ Oncology Information System with Particle Therapy License because a specific sequence can result in a partial treatment being delivered twice.
Gold Star Distribution is recalling Aleve over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.