State
73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cooper Europe is recalling specific Avon Cobra Chrome motorcycle tires because a thin innerliner may cause rapid deflation, increasing crash risk.
Daimler Trucks is recalling 2,725 Western Star 4900 and 5700 trucks because sleeper cab vent windows may detach due to improper adhesive.
Thor Motor Coach is recalling 2020 Sequence 20L motorhomes because solar panel screws may fail, causing the panel to detach and create a road hazard.
Forest River is recalling 2020 Cherokee Alpha Wolf travel trailers because an incorrectly connected wire may lack overcurrent protection, increasing the risk of fire.
Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because missing seat recliner parts may reduce occupant restraint in a crash.
Mercedes-Benz is recalling 24,226 vehicles due to a software fault that may cause the emergency call system to relay inaccurate location data, potentially delaying emergency responders.
Mercedes-Benz is recalling 29,720 vehicles because front seat belts may be incorrectly detected as unfastened, potentially disabling safety features.
Mazda is recalling specific 2007-2012 CX-7, CX-9, and 2009-2012 Mazda6 vehicles because the front passenger air bag inflators may explode, posing a risk of serious injury or death.
Gulf Stream is recalling 2020 Amerilite, Conquest, Innsbruck, Grand River, Kingsport, and Trail Master trailers because the gas refrigerator may not be properly sealed, potentially releasing carbon monoxide or flammable LP gases.
Honda is recalling 2019-2020 Pilot and 2019 Passport vehicles because front frame members may not be fully welded, potentially reducing crash protection.
Mazda is recalling specific 2003-2008 models because front passenger air bag inflators may explode, posing a risk of serious injury or death.
John Deere is recalling 4044R, 4052R, and 4066R compact utility tractors because improperly torqued front cab support bolts can fail during a rollover, posing a crushing injury hazard.
New Port Sales is recalling All-Gloo Craft Glue because the packaging does not meet child-resistant closure requirements, posing a poisoning hazard to children.
Lipari Foods is recalling Premo and Fresh Grab Ham & Cheese wheat sandwiches because they contain chicken recalled for potential Listeria monocytogenes contamination.
Lipari Foods is recalling Premo Signature Cranberry Almond Chicken Salad croissant sandwiches because the chicken may be contaminated with Listeria monocytogenes.
Lipari Foods is recalling Premo and Fresh Grab Chicken Salad wheat sandwiches because the chicken may be contaminated with Listeria monocytogenes.
Mrs. Stratton's Salads is recalling 27,787 containers of tuna salad under four brand names due to potential Listeria monocytogenes contamination.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.
Avella of Deer Valley, Inc. is recalling 808 droptainers of Povidone Iodine, 5% Ophthalmic Solution due to a lack of sterility assurance.
Altec Industries is recalling 2018-2019 aerial devices that were not stability tested according to ANSI A92.2 standards, posing a risk of collapse.
Nephron Pharmaceuticals is recalling 162 bags of Amino Acid Injection due to lack of sterility assurance and potential leaks.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for specific clinical variants.
Nephron Pharmaceuticals is recalling 1,047 bags of del Nido Cardioplegia Solution because the bags may leak, compromising sterility.
Nephron Pharmaceuticals is recalling 1,855 bags of Fentanyl Citrate and Bupivacaine HCl injection due to potential glass contamination.
Exactech, Inc. is recalling 158 Ergo 3.2mm K-wires because they may fracture at the threads and remain in the glenoid during shoulder surgery.