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.
BMW and Toyota are recalling specific 2019-2020 models because a steering tie rod may fracture, increasing crash risk. Dealers will replace the parts free of charge.
Blue Bird is recalling 2019-2021 Vision school buses because steering drag link connections may not be tightened, risking loss of control.
Lippert Components is recalling 3000 Series Frameless windows for recreational vehicles because the adhesive bond may fail, allowing glass to detach and become a projectile.
Spartan Fire is recalling one 2019 Gladiator firefighting vehicle because a disabled sleep mode on the wireless remote controller causes batteries to discharge faster than normal.
Nova Bus is recalling 2016-2019 LFS buses because the rear door obstruction safety mechanism may fail, increasing injury risk.
Lakeside Refrigerated Services is recalling approximately 42,922 pounds of ground beef products that may be contaminated with E. coli O157:H7.
Mazda is recalling 2020 CX-30 all-wheel drive vehicles because a disconnected fuel hose may leak, increasing fire and crash risks.
Mazda is recalling 2020 Mazda3 and CX-30 vehicles because front brake caliper mounting bolts may not have been tightened properly, which could reduce braking performance.
Airstream is recalling 2017-2018 Basecamp travel trailers because the entry door window adhesive may fail, allowing glass to detach and become a projectile.
Motor Coach Industries is recalling 1,067 buses because debris or water may cause excessive alternator voltage, leading to engine shutdown and increased crash risk.
Gillig LLC is recalling 6,353 aftermarket rear suspension lower control rods due to a risk of fatigue failure that could reduce vehicle handling and stability.
Keystone RV Company is recalling 428 model-year 2020 trailers because window glass may detach while moving, creating a projectile hazard.
KYMCO is recalling 2018-2019 Like 150i scooters because excessive grease on the ABS sensor may cause deterioration and system failure, increasing crash risk.
Coach and Equipment is recalling 2019-2020 Phoenix mini-buses because seat belt retractors may not secure occupants properly, increasing injury risk in crashes.
Vermeer is recalling 2020 BC1200XL and BC1500 wood chippers because wheel lug nuts may loosen, allowing the wheel to detach and increasing crash risk.
Dana Incorporated is recalling certain heavy vehicle output shafts that may not have been properly heat treated, posing a risk of shaft fracture and detachment.
FCA US LLC is recalling 2014-2017 Jeep Cherokee vehicles due to a defect in the Power Transfer Unit that may cause loss of drive or Park function.
Chrysler is recalling specific Two-Speed Power Transfer Units for Jeep Cherokee vehicles because worn splines can cause a loss of drive or Park function, increasing crash risk.
Bonnsu is recalling Miniware teething spoons because they can break in an infant's mouth, posing a choking hazard. One injury report has been received.
Lode-King is recalling one 2021 Prestige SDG semi-trailer because the load rating decal exceeds the frame's strength capability, increasing crash risk if overloaded.
Davina Wellness is recalling wintergreen essential oils because the packaging is not child-resistant, posing a risk of poisoning to young children.
Acella Pharmaceuticals is voluntarily recalling 29,304 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers products distributed nationwide in the US and Puerto Rico.
Acella Pharmaceuticals is voluntarily recalling 112,140 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers distribution across the US and Puerto Rico.
Acella Pharmaceuticals is voluntarily recalling 49,128 bottles of NP Thyroid 15 tablets because they are superpotent. The FDA classified this as a Class I recall.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.