State
73,381 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,924 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 869 (30%) are Severe.
Which agencies issued them
These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling certain 2022-2023 Coachmen Leprechaun, Freelander, and Prism motorhomes due to an improperly tightened auxiliary LPG quick disconnect that could cause a gas leak and increase fire risk.
Winnebago and Itasca motorhomes have a defective retractable awning that may extend unintentionally while driving. This can distract drivers or create a road hazard, potentially increasing crash risk.
Micro Bird is recalling 2018-2019 G5 electric school buses because improperly crimped wires in the charging port may overheat and cause a fire.
Nissan is recalling 2021 Versa and Kicks vehicles because an intermittent electrical connection in the power steering torque sensor can disable power steering assist, increasing steering effort and crash risk.
Excellance is recalling 2022 Freightliner M2 emergency vehicles because a defective circuit board can cause vehicle lighting to fail, increasing crash risk.
Cervélo USA recalls about 1,800 Model Year 2022 R5 and Caledonia-5 bicycles and 182 ST31 LT replacement stems because handlebars can slip in the stem, causing loss of control and falls. One injury from a fall has been reported.
Navistar is recalling certain 2018-2021 International HV, HX, LT, and RH vehicles because connecting rod wrist pins may crack, causing engine failure. This could lead to engine shutdown and increase the risk of a crash.
Baby Trend is recalling about 310 Cityscape Travel Jogger Strollers (Model TJ75B12A) because the parking brake can fail, creating a fall and injury risk for children. No injuries have been reported.
Plastikon Healthcare LLC has recalled Milk of Magnesia USP nationwide due to microbial contamination in non-sterile products. The affected lot (20071A) included approximately 24,400 institutional-use cups.
ThyssenKrupp Access Corp. is recalling about 16,800 residential elevators sold between 1996 and 2012 due to an entrapment hazard. Children can become trapped in the gap between exterior and interior doors, resulting in serious injury or death; one child death has been reported.
Philips is recalling BiPAP A40 respiratory support devices because motor assemblies were manufactured with nonconforming plastic that off-gases volatile organic compounds (VOCs). Approximately 1,414 units have been distributed domestically and internationally.
Daimler Trucks North America is recalling 2020-2023 Thomas Built Saf-T-Liner HDX school buses because rear side-body panels may have insufficient joint strength.
Lippert is recalling certain Utility market brake hub assemblies that may have incorrect bearings, which can overheat and cause the wheel to detach.
Philips Respironics recalls Philips BiPAP A30 respiratory devices due to motor assemblies with nonconforming plastic that off-gases volatile organic compounds (VOCs). Patients should contact the manufacturer immediately.
Plastikon Healthcare LLC is recalling 220,500 cups of antacid containing magnesium hydroxide and aluminum hydroxide due to microbial contamination.
Ford is recalling 2022 F-150 vehicles because a defective instrument panel cover may cause the air bag to deploy improperly or project fragments.
Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to microbial contamination in non-sterile products. Lot 20074A, distributed nationwide for institutional use, should not be used.
Nikola is recalling 2022 Tre BEV vehicles because improperly installed seat belt shoulder anchorages may detach during a crash, increasing injury risk.
Plastikon Healthcare LLC is recalling an antacid oral suspension distributed nationwide due to microbial contamination. Affected lots 20051A (exp. Aug. 2022) and 20088A (exp. Sep. 2022) should not be used.
Philips Respironics recalls 295 BiPAP V30 Auto respiratory devices due to motor assemblies with nonconforming plastic. These assemblies off-gas volatile organic compounds (VOCs) during device operation.
Philips Respironics is recalling OmniLab Advanced + ventilators due to motor assemblies manufactured with nonconforming plastic that releases volatile organic compounds (VOCs). The 8 affected units were distributed across the US and internationally.
Philips Respironics is recalling 85 units of the OmniLab Advanced+ ventilation device due to motor assemblies containing nonconforming plastic that off-gasses volatile organic compounds.
Philips Respironics is recalling certain Philips OmniLab Advanced+ noninvasive ventilation devices due to motor assemblies with nonconforming plastic that can off-gas volatile organic compounds (VOCs). This is an FDA Class I recall.
Plastikon Healthcare LLC is recalling 349,100 cups of Diphenhydramine HCl Oral Solution due to manufacturing process control deviations. The product was distributed nationwide for institutional use only.
Cipla is recalling 117,844 bottles of Difluprednate eye drops nationwide due to defective containers where the protective cap can break, potentially exposing the dropper tip and compromising sterility.