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.
Hawthorne Hydroponics is recalling approximately 60,000 Grower's Edge Vaporizers because they can overheat, causing burns, fires, or electrical shocks.
Kawasaki is recalling about 72,000 MULE PRO off-highway utility vehicles because debris can ignite on the exhaust manifold and oil leaks can cause fires.
Forest River is recalling 2019-2020 Berkshire and Sportscoach motorhomes because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.
Tremcar is recalling 2018-2020 406 and 407 semi-trailers because brake actuator washers may fracture, potentially reducing braking ability and increasing crash risk.
BMW is recalling 2020 models because front seat belt sensors may misread occupants, causing improper airbag and pretensioner deployment.
BMW is recalling 2020 R 1250 RT and GS motorcycles because a damaged pivot pin may loosen the final drive connection, increasing crash risk.
Toyota is recalling 38,810 2020 Highlanders because an engine control unit error may cause the vehicle to stall, increasing crash risk.
Volkswagen is recalling 2019-2020 Audi A6 vehicles with mild-hybrid technology because moisture in the starter generator may cause a short circuit and fire.
Thule is recalling Sleek Car Seat Adapters because plastic brackets can break, posing a fall hazard to infants. No injuries have been reported.
Kidz Concepts is recalling Lilly of New York children's winter boots because the soles contain lead levels exceeding federal limits. No injuries have been reported.
Grizzly Industrial is recalling about 20,645 children's tool kits because some components contain excessive lead and fail toy safety requirements. No injuries have been reported.
Crate and Barrel is recalling Miles Glass Pitchers with Wood Lid because the handle can break, posing a laceration hazard. No injuries have been reported.
Plant Therapy is recalling specific wintergreen essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning to young children.
BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.
CPSC recalls about 3,600 Kids & Koalas baby walkers sold on Amazon due to fall and neck entrapment risks.
BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.
Woom bikes USA is recalling approximately 5,500 model 4, 5, and 6 bicycles because the front fork can loosen and detach, posing fall and injury risks.
C3 Manufacturing is recalling about 1,100 Perfect Descent Auto Belay climbing devices because the belay can loosen, causing rope slack and allowing the climber to fall.
Kawasaki is recalling approximately 80,000 MULE PRO off-highway utility vehicles because excessive steering shaft wear can affect steering control, posing a crash hazard.
Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.
Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.
American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.
Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Maquet Cardiovascular is recalling Getinge 88-Series washer disinfectors because ruptured spot welds may cause water leakage, posing slip and infection risks.
Cardinal Health is recalling Monoject Hypodermic Safety Needles that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.