State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.
North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.
Meijer is recalling Salted Caramel Almonds due to undeclared peanuts. The product was distributed in six states.
North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.
KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.
North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
To Your Heart's Content is recalling Plush Puffs Marshmallows in Toasty Coconut flavor because the product contains undeclared milk.
MORryde is recalling approximately 2,500 Zero G Ramp Door hinges manufactured between August 21, 2016, and December 12, 2016, because insufficient welds may cause the door to swing down with excessive force.
Merge Healthcare is recalling eFilm Workstation software versions 2.1 through 4.1 because RF projection images may display incorrect measurements without a calibration indicator.
RaySearch Laboratories is recalling RayStation software versions 4.0, 4.5, 4.7, and 5.0 due to potential inaccuracies in proton dose calculations for specific treatment plans.
Philips Medical Systems is recalling 184 Brilliance 64 CT systems worldwide due to a software error involving the filament on timer.
DRV Suites is recalling 2017 Full House recreational trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.
Trek is recalling about 600 Bontrager Flare RT and Ion 700 RT bicycle lights because they may operate intermittently, reducing rider visibility.
Green Dirt Farm is recalling "Dirt Lover" sheep's milk cheese due to Staphylococcus aureus contamination exceeding action limits.
Philips Medical Systems is recalling 371 Ingenuity CT systems worldwide due to a software error involving the filament on timer.
Philips Medical Systems is recalling Spectral CT software due to a defect causing issues with filming, saving, and annotating images.
Green Dirt Farm is recalling Ruby blended milk cheese due to Staphylococcus aureus contamination exceeding action limits.
Philips Medical Systems is recalling 509 Ingenuity Core 128 MRI systems due to a software error involving the filament on timer.
RaySearch Laboratories is recalling RayStation 5.0 software due to a potential error in dose display on auxiliary CT images, which could result in incorrect treatment planning data.
SSI-GoPicnic LLC is recalling 1,584 cartons of Turkey Slices & Cheddar Cheese snacks labeled gluten-free because they contain wheat gluten.
Saputo Cheese USA is recalling specific lots of low moisture mozzarella cheese after a customer reported finding white plastic in the product.
Perfetti Van Melle USA Inc is recalling Airheads Mini Bars because blood was observed on packaging equipment. The recall covers 4,147 cases distributed nationwide.
Navilyst Medical is recalling Xcela Power Injectable PICC Maximal Barrier Nursing Kits because included sterile gloves have incorrect expiration dates.