State
73,104 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 729 (25%) are Severe.
Which agencies issued them
These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Motiv Power Systems is recalling 2019-2024 electric chassis vehicles because a software error may shut down high-voltage batteries, causing loss of power steering and braking.
Motiv Power Systems is recalling 2021-2024 E-450 BEV chassis vehicles because damaged CAN signal wires could cause a loss of drive power, increasing crash risk.
Doosan is recalling 2024 Bobcat PG25 portable generator trailers because improperly tightened wheel lug nuts may allow wheels to detach, increasing crash risk.
Blue Bird is recalling 2019-2023 Vision and All American school buses because roof joints may be too weak, risking panel separation in a crash.
Ford is recalling 2023-2024 Transit vehicles with the Trail package because corrosion in the steering system may cause a loss of power assist, increasing crash risk.
Ford is recalling specific front axle tie rod assemblies because incorrectly heat-treated ball studs may break, potentially causing loss of steering control.
CFMOTO is recalling approximately 3,630 ZFORCE 950 HO Sport Side-by-Side recreational off-highway vehicles from 2022–2023 because the shock absorber rod assembly can unthread and detach, causing suspension collapse and crash or tip-over hazards.
Chrysler is recalling 2017-2018 Pacifica Plug-In Hybrid vehicles because the battery pack may cause a fire while parked. Owners should park outside and avoid charging until repairs are completed.
Chrysler is recalling 2019-2021 Pacifica Plug-In Hybrids because the battery pack may cause a vehicle fire while parked. Owners should park outside and avoid charging until repairs are completed.
Hyundai is recalling 2023 Xcient vehicles because the pitman arm may not be secured properly, which can result in a loss of steering control and increase the risk of a crash.
Sassy Baby Inc. is recalling about 3,000 Manhattan Toy Brilliant Bee Rattles because the wooden base can detach and release plastic rings that pose a choking hazard to young children.
BISSELL is recalling about 3.2 million Steam Shot Handheld Steam Cleaners because they can expel hot water or steam during heating or use, causing burn injuries. The company has received 183 reports of hot water or steam escaping, including 157 reports of minor burn injuries.
Winnebago is recalling 2021–2025 Ekko motorhomes due to inadequate over-current protection in the solar charging system, which can cause the fuse to melt and increase fire risk. Dealers will replace the solar controller fuse and related components at no charge.
Honda is recalling 2024 Prologue vehicles because the right front lower control arm may contain a manufacturing defect that can fracture, causing loss of vehicle control and increasing crash risk.
The National Highway Traffic Safety Administration is recalling certain Maserati MC20 and MC20 Cielo vehicles because their tire labels show incorrect vehicle capacity weight information, potentially causing overloading risks.
Synergetics Inc is recalling Bausch+Lomb I-PACK Intravitreal Injection Kits because sterilization certificates could not be validated by the supplier. The FDA classified this as Class I.
Suntegrity IMPECCABLE SKIN sunscreen foundation is recalled for microbial contamination with Aspergillus Sydowii mold. Consumers should discontinue use immediately.
Synergetics Inc is recalling 35 units of the BAUSCH+LOMB I-PACK Intravitreal Injection Kit because sterilization certificates could not be validated, creating an infection risk.
FDA has recalled 116 units of BAUSCH+LOMB I-PACK Injection Kits because sterilization certificates could not be validated by the supplier, creating potential infection risk for patients receiving intravitreal eye injections.
Synergetics Inc is recalling the Bausch+Lomb I-PACK Injection Kit nationwide because sterilization certificates could not be validated by the supplier. The unvalidated sterilization of this eye injection device poses a potential infection risk.
American Contract Systems Inc is recalling 107 units of FOOT ANKLE-LF Procedure tray distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits for permanent-implant devices.
Cardinal Health is recalling 136,753 Presource surgical kits nationwide because included Shenli syringes contain design modifications that could cause inaccurate dosing and device leakage, risking patient harm.
Fresenius Medical Care recalls 6 blood pump rotor spare parts used in dialysis machines due to loose or dislodged guide sheaves that developed after clinical use.
American Contract Systems Inc is recalling 272 units of its TOTAL KNEE prosthesis nationwide due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component that exceed safe limits for permanent implants.
Amerisource Health Services is recalling Bupropion Hydrochloride 150mg extended-release tablets nationwide due to dissolution specification failures. The tablets dissolve faster than specified limits.