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.
Ford is recalling 2015-2017 Transit vehicles because a flexible coupling may fail, potentially damaging brake and fuel lines or allowing the vehicle to roll.
Ford is recalling 2016 Escape vehicles because the driver's knee airbag may not inflate properly in a crash, increasing injury risk.
Ford is recalling 2017 Explorer Police Interceptor vehicles because second-row seats may lack front inboard attachments, failing federal safety standards and increasing crash injury risk.
Transportation Collaborative is recalling 2012-2017 Trans Tech buses because a fuse in the air conditioning system may short, overheat, and cause a fire.
Daimler Trucks North America is recalling 2015-2017 Freightliner models because a missing check valve could cause sudden parking brake application and increase crash risk.
Volkswagen Group of America is recalling 2016-2017 Audi Q3 vehicles because brake lights may not activate during emergency braking if the parking brake is engaged.
Maxi Canada, Inc. is recalling 4.3 million pounds of frozen breaded chicken products because they may contain undeclared milk, a known allergen.
Overhill Farms is recalling approximately 54,630 pounds of frozen chicken bites products due to possible contamination with bone fragments.
The Wornick Company is recalling beef ravioli products because they may contain undeclared milk, a known allergen, which is not listed on the label.
Honda is recalling 2018 Odyssey vehicles because the third-row center seat belt tongue may not latch securely, increasing injury risk in a crash.
Forest River is recalling 2014-2018 Coachmen RV models because exposed wiring may short circuit and cause a fire.
Continental Automotive Systems is recalling fuel pump flanges for Volkswagen, Audi, and Porsche vehicles because they may crack and leak fuel, increasing fire risk.
Mazda is recalling 2014-2016 Mazda3 and Mazda6 vehicles because water may cause the parking brake actuator shaft to corrode and bind, potentially preventing the brake from engaging or disengaging fully.
Jaguar is recalling 2010-2011 XJ vehicles because a software update failure may leave air bag calibration incorrect, increasing injury risk in a crash.
The Kroger Co is recalling Simple Truth Dry Roasted Macadamia Nuts due to potential Listeria monocytogenes contamination.
Complete Pharmacy and Medical Solutions LLC is recalling 49 vials of Human Chorionic Gonadotropin due to confirmed bacterial contamination.
Aston Martin is recalling 2012 V8 Vantage vehicles because a transmission connector may break, causing a fluid leak that could prevent shifting or cause the vehicle to roll away.
Medtronic is recalling custom suture packs because an incomplete inner package seal may cause the suture material to degrade prematurely.
Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.
Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the heater head could fall and cause thermal injuries to patients.
Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.
GE Healthcare is recalling Optima CT660 and CT680 X-ray systems because a defect may cause scans to start before a prescribed delay completes.
Biomerieux Inc is recalling VITEK 2 Streptococcus Susceptibility cards because compromised container integrity may expose the product to moisture, potentially degrading antibiotic potency.
GE Healthcare is recalling Discovery IQ X-ray systems because a software issue may cause scans to start before a prescribed delay completes.