State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.
ECCO is recalling 761 LED stop, tail, turn, and reverse lights for emergency vehicles because they may be too bright, potentially affecting other drivers' vision.
Forest River is recalling 2020 Surveyor trailers because a furnace may detach from the exhaust vent, creating a carbon monoxide hazard.
The 2021 Forest River FR3 recreational vehicle has a wiring harness defect that can cause leveling jacks to deploy while driving, risking loss of vehicle control. Forest River will provide free repairs.
Certain 2020-2021 motorhomes built on Sprinter chassis may develop a brake hose chafed by the fender liner, potentially losing brake fluid. Owners should have dealers inspect and replace brake hoses and modify fender liners at no cost.
Grand Design is recalling 2016-2018 Reflection trailers because a wiring connector may allow water intrusion, potentially causing an electrical short circuit and fire.
Lochinvar is recalling about 34,300 residential boilers because a flue grommet can fail, allowing carbon monoxide to escape. Consumers should contact a technician for a free repair.
Modus Furniture is recalling Brighton, Travis, and Bevelle dressers because they are unstable without mirrors, posing tip-over and entrapment risks to children.
American Honda is recalling about 25,000 2019-2020 Pioneer and Talon off-highway vehicles because they may move while in park, posing crash and injury risks.
Dometic is recalling specific CFX3 and CFF Series chest refrigerators because a faulty protection device may cause voltage overload, electrical damage, and fire risk.
Fresenius Kabi is recalling specific lots of Ketorolac Tromethamine Injection because particulate matter was found in reserve sample vials.
Medtronic is recalling 177 Mazor X Surgical System Positioner Type II units because they may unexpectedly detach from the operating table, posing a risk of blunt injury to patients.
RaySearch Laboratories is recalling RayStation 9A software due to errors in dose calculation algorithms that could underestimate radiation therapy doses.
Endologix is recalling Ovation iX Abdominal Stent Graft Systems because a material weakness may cause polymer leaks during implantation, potentially leading to clinical events.
Fresenius Kabi is recalling specific lots of Ketorolac Tromethamine Injection because particulate matter was found in reserve sample vials.
Rexair is recalling about 38,000 Rainbow SRX vacuums because the circuit board can spark, posing fire and burn hazards. Two fires have been reported.
RaySearch Laboratories is recalling RayStation 8B Service Pack 2 software due to a defect in dose calculation algorithms that could underestimate radiation dose.
RaySearch Laboratories is recalling RayStation 5 Service Pack 3 software due to a dose calculation error that may underestimate radiation dose.
Canon Medical System is recalling 24 Infinix-8000C digital radiography systems because loose bolts may cause the catheterization table to tilt.
RaySearch Laboratories is recalling RayStation 6 Service Pack 2 software due to a calculation error that could underestimate radiation dose.
QuVa Pharma is recalling 648 bags of oxyTOCIN 30 Units/500 mL because the product did not contain the active drug.
Volkswagen is recalling one 2020 Jetta because front brake caliper bolts may come loose, potentially affecting brake performance and increasing crash risk.
Biomet is recalling A.L.P.S. Proximal Humerus Plating System Drill Block Set Screws because they were distributed without completed design history files or design transfer activities.
BioFire Diagnostics is recalling the FilmArray BCID Panel due to an increased risk of false positive Proteus results when used with specific blood culture media.
Intuitive Surgical is recalling IS4000 stainless steel reprocessing trays because small holes in the sterilization wrap could compromise sterility and increase infection risk.