State
73,806 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Navien is recalling specific tankless water heaters and boilers converted to propane due to a risk of excessive carbon monoxide production. No injuries have been reported.
Toyne Inc. is recalling 2017-2018 Fire Apparatus trucks because Whelen accessory brake lights may illuminate falsely, potentially confusing other drivers.
Chrysler is recalling 2019 Jeep Cherokee vehicles because the instrument cluster may fail, preventing warning chimes and gauges from activating, which increases crash risk.
Teva Pharmaceuticals USA is recalling specific lots of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Nissan is recalling 2009 Murano vehicles because ABS valves may fail to close properly, increasing the risk of a crash.
Daimler Trucks is recalling 2018-2019 Thomas Built Saf-T-Liner school buses because loose steering tie rod arm bolts may separate, affecting steering and increasing crash risk.
U.B.C. Food Distributors is voluntarily recalling Baraka Mild Curry Powder due to high levels of lead found in the product.
Westminster Pharmaceuticals is recalling specific lots of Irbesartan Tablets because FDA testing found traces of the NDEA impurity.
Teva Pharmaceuticals USA is recalling specific lots of Amlodipine and Valsartan Tablets 5 mg/320 mg because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Daimler Trucks North America is recalling 2018-2019 Freightliner and Western Star trucks because a clutch component may fail, causing unintended vehicle movement.
Kia is recalling 2011-2018 Optima, Sportage, and Sorento vehicles that had previous engine replacements due to a potential fuel pipe defect that could cause a leak and fire.
Teva Pharmaceuticals USA is recalling specific lots of Amlodipine and Valsartan Tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Toyota is recalling 2019 Corolla hatchbacks because pump impeller blades in the torque converter may detach, potentially causing a vehicle stall and increasing crash risk.
General Motors is recalling 2019 Cadillac XTS vehicles because a missing rivet in the front seat belt buckle may allow it to separate during a crash, increasing injury risk.
Teva Pharmaceuticals USA is recalling Amlodipine and Valsartan Tablets 10 mg/320 mg because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
ArjoHuntleigh is recalling 10 units of Passive Clip Slings because the material may break during patient transfers, posing a risk of falls and serious injury.
Teva Pharmaceuticals USA is recalling Amlodipine, Valsartan, and Hydrochlorothiazide Tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
U.B.C. Food Distributors is voluntarily recalling Baraka Hot Curry Powder in 7 oz plastic jars due to high levels of lead.
Teva Pharmaceuticals USA is recalling specific bottles of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Cedar Lake Tea is recalling Apricot Chai Tea due to potential glass contamination. The product was distributed in six states.
Westminster Pharmaceuticals is recalling specific lots of Irbesartan tablets because FDA testing found traces of the NDEA impurity.
Teva Pharmaceuticals USA is recalling specific lots of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Teva Pharmaceuticals USA is recalling Amlodipine and Valsartan Tablets 5 mg/160 mg because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because loose steering bolts may cause loss of vehicle control.
Westminster Pharmaceuticals is recalling specific lots of Irbesartan Tablets because FDA testing found traces of NDEA impurity.