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.
Ford is recalling 2017 Focus vehicles because an insufficient weld on the rear left seat back may reduce its strength, increasing injury risk in a crash.
Ford is recalling 2017 Explorer, Taurus, and Police Interceptor vehicles because steering gear heat shield fasteners may corrode and detach, potentially causing overheating and increased steering effort.
Hyundai is recalling 2017 Ioniq Electric vehicles because a manufacturing defect in the Electronic Power Control Unit may allow coolant to contact the circuit board, potentially causing a stall and increasing crash risk.
Ford is recalling 2015-2017 F-150 and 2017 F-250/F-350 trucks because the left rear inflatable seat belt buckle may detach, increasing injury risk.
Spartan Motors is recalling 2016 Utilimaster Truck Bodies because the printed tire pressure label is too low. This may cause under-inflation and tire blowouts.
Forest River is recalling 2018 XLR ToyHaulers because the Federal Placard may display incorrect tire and rim specifications, potentially leading to the installation of incorrect replacement tires.
Daimler Trucks North America is recalling 2017-2018 Western Star 4900 trucks because front axle weight capacity may exceed spring capacity, risking axle separation.
Thor Motor Coach is recalling 2018 Four Winds, Chateau, and Freedom Elite recreational vehicles because a liquid propane hose may sag and pinch, potentially causing a leak and fire risk.
Arc'teryx is recalling Procline ski mountaineering boots because a rear axis pin can dislodge, posing a fall hazard. No injuries have been reported.
Airwair is recalling Dr. Martens Vegan 1460 boots in cherry red because the tongue lining contains benzidine. Consumers should stop using the boots and contact Dr. Martens for a refund or replacement.
Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.
Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.
Truly Good Foods is recalling Blackened Seasoned Pumpkin Seeds because they were mixed with almonds and cashews, which are undeclared tree nut allergens.
NatureAll is recalling Acidophilus-Plus dietary supplements because they contain undeclared milk allergens, including colostrum, dried yogurt, and whey.
Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.
Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.
Cenorin, LLC is recalling 18 ThermaSure Series 1000 medical device dryers because a manufacturing defect causes the terminal block to overheat, char, or burn.
Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.
ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.
Boston Scientific is recalling approximately 12,450 SQ-RX 1010 Pulse Generators because memory corruption may cause the device to deliver an atypical amount of energy.
Boston Scientific is recalling approximately 16,750 Emblem S-ICD devices because they may deliver atypical energy levels due to internal memory corruption.
Toyota is recalling 2017 Highlander and Highlander Hybrid vehicles because roof rail fasteners may not be torqued properly, posing a road hazard risk.
Forest River is recalling 2018 Rockwood and Flagstaff trailers because improperly torqued spindle nuts may cause hub bearing failure and loss of vehicle control.
Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.
Nutrilife is recalling 29% hydrogen peroxide bottles because caps may not vent properly, allowing pressure to build and cause rupture, posing fire and burn risks.