State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Oridion Medical is recalling CAPNOSTREAM 20P bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
Teva Pharmaceuticals is recalling 313 bottles of Clozapine 12.5 mg tablets because routine stability testing showed the tablets failed to disintegrate as required.
Oridion Medical is recalling 56 Capnostream20 bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
Oridion Medical is recalling three Capnostream20 M bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
Otsuka is recalling 17,325 treatNOW Abilify physician sample kits due to labeling errors, including misspelled product names and missing storage instructions.
Smiths Medical ASD Inc. is recalling 13,750 Portex First Breath Nasal Oxygen Cannulas because the 'Manufactured' and 'Use By' labels are transposed, incorrectly suggesting the product expired before it was manufactured.
Smiths Medical ASD Inc. is recalling 850 Portex First Breath Nasal Oxygen Cannulas because the 'Manufactured' and 'Use By' dates are transposed, incorrectly suggesting the product expired before it was made.
Otsuka is recalling 4,738 physician sample kits of Abilify and Abilify Maintena due to labeling errors, including misspelled product names and missing storage instructions.
Dannoritzer Medizintechnik GmbH & Co. KG is recalling Instructions For Use (IFU) for certain laparoscopy instruments because the manual cleaning process was not validated.
Smiths Medical ASD Inc. is recalling 2,550 adult nasal cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expired before it was manufactured.
Smiths Medical ASD Inc. is recalling 3,000 Portex First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, suggesting the product expires before it was manufactured.
Smiths Medical ASD Inc. is recalling 12,000 First Breath Adult Nasal Cannulas because the 'Manufactured' and 'Use By' labels are transposed, incorrectly suggesting the product expired before it was manufactured.
Ford is recalling 2017-2018 GT vehicles because a rear wing valve block may leak hydraulic fluid, which can increase the risk of a fire.
Altec is recalling 2014-2018 AC40-152S cranes because the electronic load protection screen may display incorrect values, risking unit instability or loss of load control.
Altec is recalling 2017-2018 aerial devices and digger derricks because a step on the fiberglass platform can break off, increasing injury risk.
Thor Motor Coach is recalling 2,854 specific 2013 motorhome models because incorrectly installed windshield wipers may fail, reducing driver visibility and increasing crash risk.
Cracker Barrel Old Country Store is recalling decorative driftwood pineapples because sharp metal leaves pose a laceration hazard.
Marker is recalling Kingpin 10 and 13 ski bindings because steel pins can break, reducing release force and causing a fall hazard. No injuries have been reported.
Daimler Trucks North America is recalling 2019 Freightliner Cascadia and Western Star 5700 vehicles because the steering wheel may detach, risking loss of control.
Daimler Trucks North America is recalling 2018-2019 Freightliner, Western Star, and FCCC trucks because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.
Hyundai is recalling 2017-2018 Ioniq Hybrid and 2018 Plug-In Hybrid vehicles because a faulty relay may overheat the rear seat, increasing the risk of a fire.
Daimler Trucks North America is recalling 2018-2019 Thomas Built school buses because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.
Great Dane is recalling 2019 Everest CL Multi-Temp trailers because loose brake adjuster anchor pins may cause brake failure or fire.
Daimler Trucks North America is recalling 2016-2019 Thomas Built Buses Minotour school buses because the rear emergency exit door may not open wide enough to meet federal safety standards.
Truck-Lite is recalling right-hand headlights for 2016-2019 International LT trucks due to incorrect markings that may lead to improper aiming and reduced visibility.