State
73,809 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,860 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 1,974 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Multistrada is recalling specific Achilles Desert Hawk tires because the lower sidewall may separate, increasing crash risk.
Riverside is recalling one 2018 Dream trailer because the awning may deploy while moving, increasing crash risk. Dealers will replace the awning controller free of charge.
Jerky Boyz Chicken Jerky is recalling approximately 23 pounds of ready-to-eat chicken jerky products due to a processing deviation that may have led to underprocessing.
Cooper Lighting is recalling specific All-Pro and Defiant solar-powered outdoor LED light fixtures because the batteries can overheat and cause a fire.
Hyundai is recalling 2019 Santa Fe vehicles because side curtain air bag mounting bolts may damage the air bags during deployment, increasing injury risk in a crash.
Toyota is recalling 2019 C-HR vehicles because rear axle hub bearing bolts may be insufficiently tightened. This defect could damage brake components or cause a rear wheel to detach, increasing crash risk.
BMW is recalling 2016-2017 M3 and M4 vehicles because the driveshaft connection may fail, causing a loss of propulsion and increasing crash risk.
Gulf Stream is recalling 2018-2019 Conquest and B Touring Cruiser motorhomes because an unfused solar charging port circuit may increase the risk of fire.
Erwin Hymer is recalling 172 motorhomes because the generator may overcharge auxiliary batteries, potentially causing acid spills if non-sealed batteries are used.
Toyota is recalling 2018-2019 Tundra vehicles because the load carrying capacity label incorrectly overstates weight by 10 pounds, failing federal safety standards.
B. Braun Medical is recalling 1,848 Contiplex Tuohy Sets because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 6,850 clamp-style catheter connectors because they may not stay closed, causing leakage or disconnection.
Endo Pharmaceuticals is recalling 2,856 bottles of Robaxin-750 (methocarbamol) because the labels contain incorrect dosage instructions.
Endologix is notifying physicians about the AFX2 Bifurcated Endograft System due to observed Type III endoleaks. This is a follow-up to a December 2016 notification.
B. Braun Medical is recalling CE18TB epidural trays because the catheter connectors may not stay closed, causing leakage or disconnection.
B. Braun Medical is recalling 1,980 epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
Neighbors LLC is recalling 7,264 units of Crazy About Cookies Gluten Free Chocolate Chip Cookie Dough because the packaging fails to declare almonds as an ingredient.
Endologix is notifying physicians of updated surveillance recommendations for AFX endografts due to observed Type III endoleaks.
Alpha Technology is recalling mechanical key ignition switches that may shift out of the RUN position, causing the engine to turn off and increasing crash risk.
Leica Microsystems is recalling 67 automated slide stainers because a single fault could expose users to hazardous mains voltage.
Daimler Trucks North America is recalling 2018-2019 Freightliner MT45G and MT55G vehicles because an improperly tightened engine ground stud may cause overheating and increase the risk of fire.
Endologix is notifying physicians of surveillance recommendations for the AFX Endovascular AAA System due to observed Type III endoleaks.
Pfizer is recalling 12,416 vials of Elelyso (taliglucerase alfa) because loose metal ferrule crimps may compromise sterility.
Endologix is notifying physicians of surveillance recommendations for AFX Limb Extension Endografts due to observed Type III endoleaks.
B. Braun Medical is recalling CE18TKDP catheter connectors because they may not stay closed, leading to leakage or disconnection.