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.
UD Trucks is recalling one Hino engine sold as a replacement for 2008 UD1800 trucks because shifting wrist pin bushings may cause excessive cylinder wear and engine failure.
International Specialty Services is recalling NAPA and Evercraft 800lb transmission jacks because a bolt may loosen, causing the saddle to destabilize and the transmission to tip over.
Trail King is recalling 2018 Fifth Wheel Live Bottom trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.
Indiana Mills and Manufacturing is recalling Generation IV school bus seats because the buckle mount rods may fracture, increasing injury risk in crashes.
Forest River is recalling 2013-2014 Coachmen Freedom Express trailers because missing frame reinforcements may cause axle misalignment, increasing crash risk.
Hale Products is recalling retaining rings for firefighting water pumps that may corrode and fail, reducing water pressure and hindering firefighting efforts.
Forest River is recalling one 2018 Haulin' Cargo trailer because its labels may list incorrect tire pressure information, potentially causing underinflation and affecting handling.
Forest River is recalling 2018 Forester motorhomes because the Federal Placard may incorrectly state the vehicle has single rear wheels instead of dual rear wheels.
Max-Trac is recalling specific Avon Viper Stryke tires because a tread bulge or separation could cause loss of vehicle control and increase crash risk.
Kia is recalling 2014-2016 Soul and Soul EV vehicles because a pinion plug defect may allow the pinion gear to separate, potentially causing loss of steering and increasing crash risk.
Mitsubishi is recalling 2015-2017 Outlander, Outlander Sport, Lancer, and Lancer Evolution vehicles because defective relays may cause engine stalls, reduced power, or overheating.
Maserati is recalling 2015-2017 Quattroporte GTS vehicles because a fuel pump resistor may fail, causing engine stall and increasing crash risk.
Hino is recalling 3,224 trucks because worn engine parts may cause failure, increasing crash risk.
BMW is recalling 2006-2010 X3 vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.
Silver Eagle is recalling 2018 Vast-20W converter dolly trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.
Skip Hop is recalling about 130,000 Moonlight & Melodies nightlight soothers because the USB wall power adapter can break, posing an electrical shock hazard.
Medtronic Navigation is recalling Spine Referencing Instrumentation sets due to a risk that clamps may break during use, potentially leaving components in the patient's body.
Wabash is recalling 2012-2013 converter dolly trailers because fasteners may loosen, allowing the counterweight tube to detach while in motion, increasing crash risk.
America New York RI Wang Food Group is recalling approximately 63,823 pounds of pork and beef sausage products due to misbranding and an undeclared milk allergen.
Medtronic Navigation is recalling Spine Referencing Instrumentation, Double Spinous Process Clamp, Tall units due to a risk of component breakage or damage during use.
Simply Fresh Foods is recalling San Francisco Foods Seafood Salad with Greek Yogurt because the ingredient label may fail to declare milk as an allergen.
Medtronic is recalling Spine Referencing Instrumentation clamps due to a risk of breakage that could leave components in the patient's body.
Medtronic is recalling Spine Referencing Instrumentation because the clamps may be damaged if opened beyond limits, potentially leaving components in the patient.
Pfizer is recalling specific lots of Levophed (norepinephrine bitartrate) injection because a damaged sterilizing filter may have compromised sterility.
Medtronic is recalling Spine Referencing Instrumentation, Double Spinous Process Clamp, Short units because they may break during use, potentially leaving components in the patient's body.