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.
Foremost is recalling about 700 glass shower doors and panels because pivot hinges can fail, causing the glass to separate from the frame and fall or shatter.
Yamaha is recalling 2015-2018 YZFR3 motorcycles because a cracked upper radiator hose may leak coolant onto the rear tire, increasing crash risk.
Gulf Stream is recalling 2019 Vintage Cruiser recreational trailers because inner hub bearings may lack sufficient grease, risking overheating and hub failure.
McNeilus is recalling 2016-2018 trucks and Oshkosh S-Series vehicles because a CNG fuel tank valve stem may eject, posing injury and fire risks.
Forest River is recalling 2019 Salem and Wildwood recreational trailers because incorrectly wired clearance lights may not work, reducing visibility.
Luxfer Canada Ltd. is recalling One-Turn Valves (part number MPVE-250) because the valve stem may forcibly eject if the knob is turned more than one turn, posing injury and fire risks.
Ducati is recalling 2018-2019 Panigale V4 motorcycles because a timing chain tensioner may loosen, causing an oil leak that increases crash risk.
Keystone RV Company is recalling 2019 Montana recreational trailers because defective axle welds could cause the wheel assembly to detach, increasing crash risk.
Winnebago is recalling 2018-2019 Forza motorhomes because liquid propane lines may lack edge protection, creating a potential fire risk.
Heartland is recalling 2019 fifth-wheel trailers because forward reflectors may be missing, reducing visibility and increasing crash risk.
Jayco is recalling 2019 Jay Flight SLX, Jay Feather, and White Hawk travel trailers because inner wheel hub bearings may lack sufficient grease, risking overheating and hub failure.
Mercedes-Benz is recalling specific 2015-2019 models because a steering rack locknut may break, causing the steering to stick and increasing crash risk.
Mercedes-Benz is recalling 2019 E450 and E63S Wagons because the tailgate spoiler may detach while driving, creating a road hazard.
Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vehicles because a fuel hose may leak, increasing the risk of a fire.
Horizon Global is recalling specific Reese Elite Aftermarket Gooseball kits installed on Chevrolet and GMC trucks due to a risk of trailer separation.
Sciegen Pharmaceuticals is recalling Irbesartan 300mg tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 75 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because loose or missing fasteners may cause the pedestal to separate, increasing injury risk.
Beckman Coulter is recalling Cytomics FC 500 and EPICS XL flow cytometers due to a manufacturing defect on the amplifier board that may cause signal loss or drifting.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Beckman Coulter is recalling 2,549 flow cytometers worldwide due to a manufacturing defect that may cause signal loss or drifting, potentially affecting patient results.
Ford is recalling 2016-2018 Focus vehicles with 1.0L engines and manual transmissions because a clutch fracture could cause a fluid leak and fire risk.
Smiths Medical is recalling 10,440 Irrisept OR bottle assemblies because leaking containers may compromise sterility, posing an infection risk.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, USP, 300 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
TSE Brakes is recalling specific Air Brake Actuators because mounting washers may fracture, potentially reducing braking ability and increasing crash risk.