State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Akorn, Inc. is recalling 31,812 bottles of Atropine Sulfate Ophthalmic 1% Solution because testing revealed low viscosity results.
AstraZeneca is recalling 18,056 bottles of Lynparza (olaparib) capsules 50 mg due to elevated levels of a specific quality attribute.
Amazon is recalling about 260,000 portable power banks because the batteries can overheat and ignite, posing fire and chemical burn risks.
MAAX Spas is recalling about 550 hot tubs and swim spas in the U.S. because the internal UV generator can ignite, posing a fire hazard.
Honda is recalling 2014-2016 Odyssey vehicles because the second row left outboard seatback may fail to lock, increasing injury risk in a crash.
Helvetia Sports is recalling SwissStop EXOTherm cycling disc brake pads because they can separate from the backplate, posing a fall hazard to users.
Autocar is recalling 1,320 Xpeditor vehicles equipped with factory-installed methane detection systems because inadequate circuit protection may cause the wiring harness to overheat, increasing the risk of a fire.
Ford is recalling 2013-2016 Focus and Fusion vehicles with manual transmissions because the clutch may fracture, causing transmission damage and fluid leaks that could lead to fire.
Daimler Trucks North America is recalling 9,480 Freightliner Custom Chassis vehicles due to a power steering hose defect that may cause electrical arcing and fire.
Ford is recalling 2014-2018 Fusion and Lincoln MKZ vehicles because the steering wheel bolt may loosen, allowing the wheel to detach and causing loss of control.
Hyundai is recalling 2016-2018 Sonata Plug-In Hybrids because a voltage protection device may activate inadvertently, causing loss of power and increasing crash risk.
SynTec Seating Solutions is recalling S3B Non-Restraint Wall Mounted Seats because the mounting bracket may crack, increasing injury risk in a crash.
Forest River is recalling 2018 Stealth Evo recreational trailers because the federal placard lists incorrect tire sizes. This error could lead owners to install wrong replacement tires, increasing crash risk.
Ferrari is recalling 2016 488 GTB and 488 Spider vehicles because a software error may prevent drivers from receiving warnings about critically worn brake discs.
Supreme Corporation is recalling 2003-2018 trucks equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.
Chrysler is recalling 2009-2012 Dodge Ram 1500 trucks in 21 states and D.C. because a fuel tank bracket may corrode, causing the tank to drop and leak fuel.
Volkswagen is recalling 2018 Tiguan long wheel base vehicles because engine support bolts may not be properly tightened, which could lead to engine breakdown or loss of power.
Kia is recalling 2017-2018 Optima hybrid vehicles because a voltage protection device may activate inadvertently, causing a loss of power in EV mode and increasing crash risk.
BDA is recalling Golden State Warriors Menorahs because the glue holding the candleholders can melt, causing lit candles to fall and posing fire and burn risks.
American Technology Components is recalling specific 7-Way Wiring Harnesses used for aftermarket truck cap installations because the wiring may overheat, increasing the risk of a fire.
AuroMedics Pharma LLC is recalling 6,072 bags of Levofloxacin in 5% Dextrose Injection because they contain visible particulate matter identified as mold.
Kareway Products Inc. is recalling 60,000 bottles of Gericare Eyewash because testing confirmed the presence of Achromobacter xylosoxidans bacteria.
Seggiano Artichoke & Garlic Sauce & Spread is being recalled because it was mislabeled and contains undeclared cashews.
Ventana Medical Systems is recalling Hematoxylin II and specific HRP dispensers due to increased reports of leaking and sticking.
Zimmer Biomet is recalling 337 femoral intramedullary nail loaner kits because the bolt connecting the insertion guide to the nail can fracture during insertion.