State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Vans USA is recalling 2016 Mercedes-Benz Metris vehicles because front seatbelt pretensioners may not function properly in a crash, increasing injury risk.
Thor Motor Coach is recalling 2017 Palazzo 36.1 and 36.3 motorhomes because the federal certification label lists an incorrect front tire rim size, which could lead to unsafe driving conditions if the rim is replaced based on that error.
Altec is recalling 2004-2005 aerial devices and elevators because the fiberglass upper boom may fail without warning, increasing the risk of serious injury or death.
Forest River is recalling 2007-2011 Cherokee recreational trailers because incorrect Federal Placards list higher weight ratings than the actual capacity, increasing the risk of overloading and crashes.
Forest River is recalling 2017 Rockwood and Flagstaff recreational vehicles because the Federal Placard may display an incorrect Gross Axle Weight Rating, which could increase crash risk.
Mitsubishi is recalling 35,674 2016 Outlander and Outlander Sport vehicles because door latches may not secure in high temperatures, increasing injury risk.
Micro Bird is recalling 2016-2017 G5 school buses with specific propane kits because a fuel valve may short circuit, causing the engine to shut off while driving.
Xootr is recalling about 3,000 adult kick scooters because the steer support can break during normal use, posing a fall hazard.
Marin Mountain Bikes is recalling 2016 and 2017 Pine Mountain bicycles because the front forks can bend or break, posing fall and crash hazards.
Lipari Foods is recalling Old Tyme Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Pepper Jack Cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Copper wood Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Hot Pepper Cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Colby Jack Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Saputo Cheese USA is recalling Dutchmark Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.
Lipari Foods is recalling Old Tyme Colby Jack Cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Copperwood Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling specific lots of Old Tyme Colby Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Colby Cheese due to potential Listeria monocytogenes contamination from a supplier.
Lipari Foods is recalling Old Tyme Swiss Cheese due to potential Listeria monocytogenes contamination from a supplier.
Saputo Cheese USA is recalling Great Midwest Applewood Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.
Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.
Lipari Foods is recalling Old Tyme Colby Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Claris Lifesciences Inc. is recalling 72,072 units of Metronidazole Injection, USP, 500 mg/100 mL, due to a potential leak that may compromise sterility.