State
73,598 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,592 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 9,592 recalls whose distribution notice names Indiana specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 31 Dual Mobility Vivacit-E bearings because the outer package label indicates a different size than the implant inside.
Brainlab AG is recalling Ultrasound Navigation Software 1.0 and related integration software because the system does not support modifying the probe's image width.
Siemens Healthcare Diagnostics is recalling Dimension LOCI High Sensitivity Troponin I reagent cartridges due to positive bias in test results.
Hormel Foods is recalling Skippy Super Chunk Peanut Butter because aflatoxin levels were slightly above the actionable limit.
VistaPharm is recalling Nystatin Oral Suspension because one lot failed impurity specifications. The affected product was distributed nationwide.
Pharmaceutical Associates Inc. is recalling Citalopram Oral Solution due to high impurity levels found during stability testing.
Hyundai is recalling 2019-2020 Kona Electric vehicles because the lithium-ion battery may short-circuit, increasing the risk of a fire.
Diode Dynamics is recalling specific SL1 LED headlamp bulbs that exceed brightness standards and may cause glare to oncoming drivers, increasing crash risk.
Shyft Group is recalling 2020 Utilimaster Walk-In vans because the throttle pedal may get trapped by the floor tread plate, increasing crash risk.
Mercedes-Benz is recalling two 2020 GLE 350 vehicles because the driveshaft locking ring may not be installed correctly, potentially causing a loss of power transfer and vehicle stall.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because the window air bag may not be mounted correctly, increasing injury risk in a crash.
Mercedes-Benz is recalling 2020 GLE and GLS models because a faulty electrical ground connection may cause power steering, wiper, or headlight malfunctions.
Westinghouse Lighting is recalling about 3,000 Great Falls outdoor ceiling fans because the blades can crack and break, posing an impact injury hazard.
The Toro Company is recalling 2017-2020 model 22618 and 22618HD Log Splitters because tow pole mounting plates could bend, causing bolts to break and increasing crash risk.
Chrysler is recalling specific Mopar driver side mirror glass parts that may detach from the backing plate, reducing visibility and increasing crash risk.
Land Rover is recalling 2010-2011 Range Rover Sport vehicles because the rear spoiler cover may detach, creating a road hazard and increasing crash risk.
Harley-Davidson is recalling 2020 LiveWire motorcycles because a software issue may cause the electric powertrain to shut down unexpectedly, increasing crash risk.
Chrysler is recalling 2020 Ram 1500 and 2500 vehicles because the driver-side mirror glass can detach, reducing visibility and increasing crash risk.
4e Brands North America is recalling blumen hand sanitizer bottles due to methanol contamination and ethanol levels below the labeled claim.
4e Brands North America is recalling Blumen Advanced Hand Sanitizer because testing found methanol contamination and ethanol levels below the labeled claim.
4e Brands North America is recalling Blumen hand sanitizer bottles and pumps found to contain methanol and less ethanol than labeled.
Riverpoint Medical is recalling 1,875 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
CB2 is recalling Bordo and Bordo XL dining tables because the legs can become unsteady, causing the table to collapse and posing an injury hazard.
The FDA is recalling specific lots of Endo GIA Auto Suture Universal Articulating Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Riverpoint Medical is recalling 1,268 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.