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.
Fisher-Price is recalling all Rock 'n Play Sleepers because over 30 infant fatalities have occurred. Consumers should stop using the product immediately and contact the company for a refund.
Honda is recalling specific 2018-2019 Acura and Honda vehicles because timing belt teeth may separate, potentially causing an engine stall and increasing crash risk.
Honda is recalling 2018-2019 Odyssey vehicles because loose battery connections may cause the transmission to shift to Park, potentially damaging the parking rod and increasing crash risk.
Forest River is recalling 2019 Dynamax Isata motorhomes because brake hoses may lack anti-corrosion plating, risking fluid leaks and loss of braking.
Cush Corp is recalling specific trailer suspension systems because a locking device may not be installed properly, allowing the wheel end to separate from the axle.
SMC Trailers is recalling 2019 Laramie horse trailers because entry steps may break due to poor welds and missing rivets, increasing injury risk.
Chrysler is recalling 2013-2016 Dodge Dart vehicles with 6-speed automatic transmissions because the shifter cable bushing may fail, allowing the cable to detach and increasing crash risk.
Karma Automotive is recalling 2018 Revero vehicles because side curtain air bags may not deploy in a rollover crash due to a disabled sensor system.
Subaru is recalling specific 2005-2014 models because a broken spring in the ignition switch could cause the engine to turn off unexpectedly, increasing crash risk.
DICK'S Sporting Goods is recalling Field & Stream Timberline Hang On tree stands because the seat weld can break, posing a fall hazard.
Forest River is recalling 2018 Dynamax Isata vehicles because the brake transmission shift interlock pin may stick, allowing the vehicle to be shifted out of park without the brake pedal or key.
Specialized is recalling about 63,000 bicycles because the steerer tube collar can crack, causing sudden loss of steering control and posing fall and injury hazards.
Daimler Vans USA is recalling 2016-2017 Metris vans in 24 states and DC because aluminum power steering bolts may corrode and fracture, causing loss of steering assist.
Legacy Pharmaceutical Packaging LLC is recalling Losartan Potassium Tablets, 50 mg, because an impurity was detected. The recall covers 179,544 bottles distributed in Arizona, Indiana, and Tennessee.
BMW is recalling 2019 X3 and X4 vehicles because the instrument panel may be improperly manufactured, potentially preventing the passenger air bag from deploying.
Better Made Snack Foods is recalling 660 bags of Original Potato Chips due to undeclared milk. The product was sold in Michigan, Ohio, and via mail order nationwide.
Chrysler is recalling 2019 Jeep Renegade and Fiat 500X vehicles because incorrect software may disable passive safety features, increasing injury risk in a crash.
Spartan Motors is recalling 2012-2018 Utilimaster Reach vehicles because improper electrical grounding may cause windshield wipers to stop working, reducing visibility.
KTM and Husqvarna are recalling about 780 model year 2019 50 SX and TC 50 motorcycles because the throttle can stick open, posing a crash hazard.
Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws due to a potential packaging error where 30mm screws may be labeled as 20mm and vice versa.
Century Snacks LLC is recalling Snak Club Honey Bliss Nut Mix because the Honey Butter Seasoning contains milk, a major allergen, that was not declared on the packaging.
Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws because 30mm screws may have been packaged as 20mm screws, and vice versa.
Zimmer Biomet is recalling 89 units of the Small Diameter Cement Plug Inserter due to a lack of adequate sterilization validation.
Beckman Coulter is recalling UniCel DxC clinical systems where a software scheduling error can cause sample mishandling and generate incorrect test results.
North Central Emergency is recalling 2016-2018 ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.