State
73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling certain 2024 GMC Canyon vehicles because the headlights may flicker while driving or parked, reducing visibility and increasing crash risk. Dealers will replace the headlight module at no cost.
Jaguar is recalling 2024 F-Pace vehicles because the Near Field Sensing Module may overheat, preventing the rearview camera from displaying and increasing crash risk.
Kawasaki is recalling 2024 Z7 Hybrid and Ninja 7 Hybrid motorcycles because the electronic control unit may cause the transmission to shift into neutral, increasing crash risk.
MJKSARE high chairs are recalled due to excessively wide leg openings that pose an entrapment hazard to infants and a fall hazard from a disengageable tray. About 4,760 units sold on Amazon from February to March 2024 are affected.
Chrysler is recalling 2018-2024 Jeep Wranglers due to a wiring harness defect that may disable the rearview camera display and center brake light, increasing crash risk.
Altec is recalling 2023-2024 Aerial Device, Digger Derrick, and Pressure Digger vehicles due to an overloaded chassis ignition circuit that can cause engine shutdown and increase crash risk.
The rearview camera image may not display on certain 2024 Land Rover vehicles due to a faulty Near Field Sensing Module that can overheat. Dealers will replace the module at no cost.
Maserati is recalling 2024 GranTurismo and GranCabrio vehicles because body control module software may display incorrect fuel levels, potentially causing engine stalls.
General Motors is recalling certain 2023-2024 trucks and SUVs because the brake fluid warning light may fail to display, potentially causing unsafe driving conditions with low brake fluid.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for the Trilogy Evo Universal Ventilator to address safety issues identified in earlier recalls. Affected units should implement the update.
Trail King is recalling 2019-2020 TKHDG Paver Special trailers because the gooseneck lift lower cylinder mount may crack, causing the trailer to drop suddenly.
Storyteller Overland is recalling 2024 GXV Hilt vehicles because the spare tire mount may not be secured properly, allowing the tire to detach.
Tiffin is recalling 2022–2025 Allegro Bay motorhomes due to subframe truss collapse that can pinch electrical wiring and cause electrical arcing, increasing fire risk.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo EV300 ventilators to resolve previously identified safety issues. Approximately 90,910 US units and 56,273 international units are affected.
Baxter Healthcare Corporation is recalling 44,208 containers of Heparin Sodium in Sodium Chloride Injection nationwide after endotoxin testing revealed out-of-limit results. The contamination poses a risk of serious adverse reactions in patients receiving the intravenous medication.
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo ventilators worldwide to resolve identified safety issues. Users must apply the update and review the updated User Manual.
Breas Medical is recalling the Vivo 45 LS ventilator due to potential elevated formaldehyde emissions into the patient breathing airpath under specific conditions.
Unilever North America is recalling Popsicle Jolly Rancher Frozen Confection Pops nationwide due to undeclared milk, which poses a risk to consumers with milk allergies.
Abiomed is updating labeling for Impella 5.5 cardiac support pumps to include information about a potential device interaction with Shockwave Coronary IVL Catheters during coronary interventions.
Reser's Fine Foods is recalling 7 cases of Smokehouse Potato Salad due to potential spoilage from temperature abuse during shipping. No illnesses have been reported.
Reser's Fine Foods is recalling Reser's American Classics Scalloped Potatoes because a refrigeration unit malfunction caused temperature abuse during shipment, potentially leading to spoilage. Consumers should not consume this product.
Abiomed is updating labeling for the Impella 5.5 SmartAssist S2 cardiac assist device to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions.
The FDA is recalling Impella CP Smart Assist Sets due to a potential device interaction with Shockwave Coronary IVL Catheters used during coronary interventions. Abiomed will update device labeling to inform users about this interaction.
Abiomed's Pump 381 Pump Set labeling lacks information about potential interactions with Shockwave Coronary IVL Catheters during coronary interventions. The manufacturer is updating instructions for use to address this gap.
Beckman Coulter is recalling 17 DxI 9000 Access Immunoassay Analyzers due to cracks in the Internal Wash Buffer Tank that can cause leaking, potentially delaying test results and exposing users to chemical and physical hazards.