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.
Lupin Pharmaceuticals is recalling 24,180 bottles of Fluocinolone Acetonide Topical Solution due to elevated impurities.
Tyson Foods is recalling approximately 36,420 pounds of chicken nuggets that may contain rubber. Consumers should not eat the product and should discard it or return it to the store.
Proterra is recalling 2015-2018 Catalyst 40 transit buses because missing air brake components may allow moisture buildup, potentially leading to brake failure.
Honda is recalling 2015-2019 Acura and Honda vehicles because fuel pump particulates may cause engine stalls, increasing crash risk.
Dynamic Tire Corp. is recalling specific Sailun tires because their sidewall markings lack the date of manufacture, failing federal safety standards.
Gillig is recalling 2016-2018 Low Floor buses because a steering draglink ball stud may not be properly tightened, increasing crash risk.
Keystone RV is recalling 2019 Montana trailers because a kitchen slide adjustment bolt may contact the tire, potentially causing tire failure and increasing crash risk.
Stoughton is recalling 2016-2019 DVW trailers because the forward attachment points for the pintle mounting assembly may crack, potentially causing the trailer to detach from the tow vehicle.
Volkswagen Group of America is recalling 2013-2016 Audi A8 and S8 vehicles because a fuel supply line may leak, increasing the risk of fire.
Chrysler is recalling specific Ram 2500 and 3500 trucks because a steering component may loosen, potentially causing loss of steering control.
Chrysler is recalling 2019 Ram 1500 vehicles because an improperly secured battery ground fastener may cause loss of power steering assist, increasing crash risk.
Honda is recalling 2017-2019 Ridgeline trucks because exposure to acids can crack the fuel pump feed port, creating a fire hazard.
Mack Trucks is recalling 2019-2020 Anthem, Granite, and Pinnacle vehicles because the passenger-side door mirror may detach, posing a risk of injury or crash.
Chrysler is recalling 2019 RAM 1500 trucks with 12-inch touchscreens and base HVAC systems because the windshield defroster does not work, increasing crash risk.
Acura is recalling 2014-2019 ILX vehicles because a deformed fuel tank may cause the fuel gauge to display inaccurate levels, potentially leading to stalling and crashes.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.
Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.
Arthrex is recalling Nano Corkscrew FT Suture Anchors because they may break during insertion. The recall covers 1,418 units distributed in the US and abroad.
Forest River is recalling 2018 XLR recreational trailers because they lack liquid propane and carbon monoxide detectors, posing an injury risk.
Carrier is recalling ComfortPro 210STA and PC6112 auxiliary power units because a second power supply harness lacks a ground fault circuit interrupter, increasing injury risk.
Kimberly-Clark is recalling U by Kotex Sleek tampons because they may come apart upon removal. The recall covers 68,852,076 units distributed nationwide and in Canada.
Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Screw Caddies due to a potential for silicone shedding during cleaning and sterilization.
Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.
Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Tray Bases because they may shed silicone during cleaning and sterilization.
Meridian Bioscience is recalling Premier Cryptococcal Antigen kits because an enzyme reagent may not maintain stability, potentially causing false negative results.