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.
CooperSurgical is recalling 1,740 units of Dilator/Sound Sets because the sterile pouch seal may be compromised, potentially affecting sterility.
GE Healthcare is recalling Giraffe Shuttle upgrade kits because the batteries emit a strong sulfur odor during charging.
Jindilli Beverages LLC is recalling 2,981 cases of Milkadamia Salted Buttery Spread due to the potential presence of mold.
CVS Pharmacy is recalling Maximum Strength Lidocaine Cold & Hot Patches because manufacturing records and samples were lost, meaning the product may not remain within specification through its expiration date.
West-Ward Columbus Inc. is recalling Doxycycline Hyclate 100 mg tablets because they failed a dissolution test at the end of their shelf life.
Inpeco S.A. is recalling 37 FlexLab Automation Systems due to a firmware communication error that can cause sample tubes to be incorrectly associated with carriers.
Jubilant Cadista Pharmaceuticals is recalling Lamotrigine Tablets, 150 mg, due to the presence of foreign silica granules consistent with desiccant pack material.
Bentley is recalling 1,892 2019-2020 Bentayga vehicles because a fuel line connector may leak, increasing the risk of fire.
Keystone RV Company is recalling 2020 Springdale trailers because they were equipped with incorrect axles and tires, which may cause the trailer to be overloaded and increase the risk of a crash.
Vee Tyre is recalling 522 Taiga A/T tires because the sidewall may separate, increasing the risk of a crash.
Forest River is recalling 2020-2021 US Cargo, Haulin', and Trail & Sport cargo trailers because safety chains may break if the trailer becomes unhitched.
Braun Ambulances is recalling 2019 Chief XL and Liberty ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
General Motors is recalling 2019-2020 Chevrolet 4500HD, 5500HD, and 6500HD trucks because the ABS malfunction light may fail to illuminate, increasing crash risk.
Frazer is recalling 2019-2020 emergency vehicles on RAM 4500 and 5500 chassis because rear brake lines may wear, causing brake failure and increasing crash risk.
Honda is recalling specific 2018-2020 models because a faulty fuel pump may cause the engine to stall while driving, increasing crash risk.
Nestle Prepared Foods is recalling Lean Cuisine Fettuccini Alfredo products because they contain undeclared soy and chicken, which are not listed on the label.
Thor Motor Coach is recalling 566 2020 motorhomes because a fender liner may chafe the brake hose, potentially causing brake fluid loss and increased braking distance.
Nissan is recalling 2013-2018 Altima vehicles because the secondary hood latch may corrode and fail, potentially allowing the hood to open while driving.
Keystone RV Company is recalling 2020 Springdale trailers because the Federal Identification Tag lists incorrect tire load range and size, which could lead to tire overinflation or overloading.
K2M, Inc. is recalling Aleutian Lordotic Spreaders because the welded tips may break off during spinal procedures.
K2M, Inc. is recalling the Aleutian Lordotic Spreader because the welded tip may break off during spinal procedures.
Bovie Medical Corporation is recalling Renuvion/J-Plasma Precise Open Handpieces because unexpected stress fractures may cause the shaft to fragment during clinical use.
Kawasaki is recalling 2019-2020 Ninja ZX-10R motorcycles because engine backfires may damage valves and cause a fire.
K2M, Inc. is recalling the Aleutian Lordotic Spreader because the welded tip may break off during spinal procedures.
K2M, Inc. is recalling the Aleutian Anatomically Narrow Lordotic Spreader because the welded tip may break off during spinal procedures.