State
73,478 recalls have nationwide distribution and so reach Indiana. 9,589 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,589 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,589 recalls whose distribution notice names Indiana specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Vicinity Motor Corporation is recalling 2020-2021 Vi38 vehicles because the power steering gear box may become damaged, resulting in a loss of steering control.
Daimler Trucks North America is recalling 2020-2023 Thomas Built Buses Saf-T-Liner EFX school buses because passenger seat mounting bolts may break, increasing injury risk in a crash.
Norco Industries is recalling certain frames with Model CA-5400 couplers due to improper welding that may cause trailer separation.
Ford is recalling 2016-2018 F-150, 2016-2017 Expedition, and Navigator vehicles because a brake master cylinder leak may reduce front brake function and increase crash risk.
Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.
The bolt securing the intermediate steering shaft to the steering gear box may become loose, potentially causing loss of steering control and increased crash risk. Ford is replacing the bolts for free.
The high voltage battery in 2021-2022 Ford Escape and 2022 Lincoln Corsair hybrid vehicles may fail, causing sudden loss of drive power and increasing crash risk.
Altec is recalling 2016-2021 aerial devices because improperly secured fuel line clamps may cause leaks and increase fire risk.
Keystone is recalling 2021-2022 Sprinter and Bullet models plus multiple 2022 travel trailer and fifth-wheel variants due to faulty solar controller wiring that can disable carbon monoxide and propane gas detectors.
Ford is recalling 2021-2022 Edge vehicles with a software error that may cause the rearview camera to display a blank or distorted image. This reduces driver visibility behind the vehicle, increasing crash risk.
Altec is recalling 2017-2021 SK185-MP and SKC landscaping spray vans because they lack carbon monoxide detectors, increasing the risk of injury from undetected gas.
Ford is recalling 2021 F-150 vehicles because the front windshield wiper motor may fail, reducing visibility and increasing crash risk.
Chrysler is recalling certain 2021 Dodge Durango vehicles because the ABS control module software may prevent the electronic stability control malfunction indicator light from illuminating, increasing the risk of crashes.
General Motors is recalling 2022 GMC Hummer EV Pickups because taillight software may cause lights to fail or stay on, increasing crash risk.
Chrysler is recalling Mopar Anti-lock Brake System (ABS) Control Modules because software may prevent the Electronic Stability Control (ESC) malfunction light from illuminating, increasing crash risk.
Vadilal Industries is recalling Quick Treat Custard Apple Pulp (1kg packages, UPC 8901777282168) due to potential Salmonella contamination. Approximately 997 cases were distributed nationwide to retail stores.
Respironics California is recalling 294 V60 Plus ventilators assembled with expired adhesive. The adhesive may fail, causing the bracket to loosen and damage capacitors, potentially stopping ventilation delivery.
Maintainer is recalling 2021-2022 crane-equipped truck bodies because an inductor may contact the frame, causing an electric arc and increasing fire risk.
A limited number of Philips Respironics V60 ventilators were assembled with expired adhesive. If the adhesive fails, the ventilator could stop providing ventilation.
Olight is recalling about 215,100 M2R Pro and Warrior Mini flashlights because they can turn on accidentally and overheat while stored in a holster or pocket, creating a burn hazard. The company has received 127 reports of unintended activation with 22 burn injuries, including three second-degree burns.
Sunstar Americas is recalling BUTLER Clear Dip nationwide due to lack of FDA premarket clearance. The product was distributed in 22,514 units across multiple lot codes.
BioPro Titanium MPJ toe implants are recalled due to false documentation claiming MRI safety testing that was never performed. Patients should not undergo MRI with this implant until properly evaluated.
Orthosoft's NavitrackER knee navigation system may lack proper sterilization. The product was distributed without passing required sterilization tests, risking infection.
BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.
Shimadzu recalled 28 Digital Angiography Systems with Generator Model D150GC-40 due to inadequate installation adjustment criteria that may cause x-ray radiation dose rates to exceed safe fluoroscopic imaging limits.