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.
Entegra is recalling 2019 Anthem, Aspire, Cornerstone, and Insignia motorhomes because improperly adjusted entry door latch rods may allow the door to open during transit.
Jayco is recalling 2019 Jay Flight travel trailers because incorrectly wired turn signal and brake lights may fail to operate, increasing crash risk.
Winnebago is recalling 2017-2019 Minnie Drop trailers because a missing clamp may allow the propane line to contact the refrigerator burner, posing a fire risk.
Mercedes-Benz is recalling certain 2016-2018 GLC models because rear seat belt latch plates may retract into the interior paneling, preventing use.
UberScientific is recalling Uber Numb topical anesthetic cream and spray because the packaging is not child-resistant, posing a risk of poisoning to young children.
Chrysler is recalling 2018-2019 Jeep Wranglers because improperly welded front track bar brackets may separate, reducing steering capability and increasing crash risk.
BMW is recalling 2019 X6 and X6 M vehicles because improperly hardened rear suspension bolts may break, increasing crash risk.
KZRV is recalling 2017-2019 Sonic 190VRB travel trailers because the liquid propane manifold may be located close to the axle tube, posing a fire risk.
Boy Story is recalling Mason and Billy action dolls because the vinyl joints can break, creating pieces that pose a choking hazard to young children.
Integrated Tower Systems is recalling 2007-2018 Mobile Tower trailers because a missing power disconnect on the control panel may cause electrical shock.
Honda is recalling 2010-2014 Ridgeline, Element, and Acura RL vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.
Forest River is recalling 2019 Flagstaff and Rockwood recreational trailers because incorrectly oriented brake mounting flanges may cause premature brake failure, increasing crash risk.
Life Fitness is recalling about 11,800 PowerMill climbers because liquid entering the power receptacle can cause electrical arcing, sparking, and fire.
Honda is recalling specific 2010-2015 models because the passenger frontal air bag inflator may explode, potentially causing serious injury or death.
Honda is recalling 2019 Insight, Odyssey, and Ridgeline vehicles because a manufacturing error in the SRS control unit may prevent air bags or seatbelt pretensioners from deploying in a crash.
Honda is recalling 2017-2018 Civic and CR-V vehicles because a loose magnet in the electric power steering system may cause unintended steering input, increasing crash risk.
TerraTrike is recalling 600 adult tricycles because the right wheel hub mount can bend or break, creating a crash risk.
IKEA is recalling CALYPSO ceiling lamps because the glass shade can detach and fall, posing impact and laceration hazards. Consumers should stop using the lamps and return them for a refund or replacement.
QuVa Pharma is recalling 528 bags of Norepinephrine 4 mg in 5% Dextrose because the active ingredient may be missing. The product was distributed to hospitals nationwide.
Pro-Med Instruments is recalling 31 DORO LUCENT Transitional Members because mixing design revisions may cause the headrest system to malfunction.
Pro-Med Instruments is recalling 30 DORO LUCENT Headrest Systems because mixing design revisions may cause malfunction during surgery.
Daimler Trucks North America is recalling 2017-2019 FCCC MC motorhome chassis because primary and secondary air lines were incorrectly connected to the pressure gauges, increasing crash risk.
Fresenius Medical Care is recalling 80 hemodialysis systems because a power failure during cleaning may allow disinfectant to remain in the machine and be delivered to patients.
Pro-Med Instruments is recalling 31 DORO LUCENT Locking Transitional Members because mixing design revisions may cause the headrest system to malfunction.
Beaumont Bio-Med, Inc. is recalling 90 bottles of Sinus Response Homeopathic Formula due to manufacturing deviations that could result in microbial contamination.