State
73,092 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 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling 2024-2025 Viking and Clipper travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.
Ford is recalling certain 2024 F-53 and F-59 stripped chassis vehicles because the instrument panel cluster may not properly display the transmission gear position indicator, failing FMVSS 102.
Royal Enfield is recalling certain 2023 Himalayan, Classic 350, Meteor 350, Hunter 350, Super Meteor 650, Int 650 and Continental GT 650 motorcycles whose side and rear reflectors fail FMVSS 108.
Deere & Company is recalling about 147,900 John Deere 1023E, 1025R, and 2025R Compact Utility Tractors because the front bell crank in the brake linkage can fail, causing loss of braking and crash risk. Four failures have been reported, including one hospitalization and two impact injuries.
Brinkley RV is recalling certain 2025 Model Z travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating. 40 units are affected.
Tesla is recalling certain 2024 Cybertruck vehicles because the rearview camera image may be delayed after shifting into reverse, failing FMVSS 111. 27,185 units affected.
Harley-Davidson is recalling 2018-2019 Softail FXBB and FXLR motorcycles because the front tire inflation pressure on the VIN label may be incorrect, potentially leading to tire overloading.
Chrysler is recalling 2024 Ram Promaster BEV vehicles because incorrect software may cause a loss of drive power, increasing crash risk.
Liberty Hardware is recalling about 174,500 Multi-Grip Tub Safety Bars because plastic grip pads can become dislodged on tapered tubs, making the bars unstable and creating a fall hazard. One minor fall injury has been reported.
BMW is recalling specific 2024-2025 models because the steering spindle may break, increasing steering effort and crash risk. Dealers will replace the joint free of charge.
BMW is recalling certain 2023-2024 228i, 228i xDrive and 2025 MINI Countryman S ALL4 vehicles because the bolts connecting the front body structure to the chassis may be loose.
Bliss Tree Millet Butter Murukku products are being recalled due to undeclared sesame and milk allergens. Affected products were distributed to retailers and online customers in multiple states.
Tenneco is recalling aftermarket ball joints for 2013-2019 Ford Escape vehicles because they may separate, causing loss of steering control.
CareFusion's Alaris Syringe Module Model 8110 infusion pumps are being recalled because affected units may have bent female connectors that can prevent device operation and delay infusions. Approximately 20,145 units have been distributed worldwide.
PHILIPS medical X-ray imaging systems may have a cable hose carrier that can detach due to broken plastic or bolts, potentially causing parts to fall and injure clinical staff.
CareFusion 303, Inc. recalls 180 Alaris EtCO2 Module Model 8300 units with potentially bent female connectors that may prevent device operation, risking delays in infusion and monitoring.
GE Healthcare is recalling three ViewPoint imaging systems due to a software vulnerability in Mirth Connect that could allow unauthorized access and manipulation of patient data.
Bliss Tree Ragi Butter Murukku 200g and 400g packages are recalled due to undeclared milk. Consumers with milk allergies should not consume these products and contact their retailer.
Siemens Healthcare's ADVIA Chemistry Microalbumin diagnostic test may produce falsely low results. Eight lots do not meet High-Dose Hook Effect and Prozone Effect specifications, potentially affecting microalbumin detection accuracy.
Tornier, Inc. is recalling one lot of the Stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS shoulder implant due to bacterial endotoxin exceeding safety specifications. The 5 affected units were distributed in Illinois, Wisconsin, Arizona, Nevada, and South Dakota.
Mazor Robotics is recalling 94 Mazor X surgical navigation devices due to software errors that cause screen lag or screw-tracking mismatches during orthopedic procedures.
B Braun's STREAMLINE FRESENIUS bloodline tubing used in hemodialysis may have a design issue where incomplete insertion of the patient connector prevents proper blood flow during certain procedures. Patients receiving dialysis may experience treatment delays.
B. Braun Medical is recalling STREAMLINE LONG hemodialysis bloodline tubing because the patient connector may fail to fully insert into the Locksite, potentially causing blood flow obstruction during dialysis treatment.
GE Healthcare ViewPoint 6 medical imaging systems contain a software vulnerability (CVE-2023-43208) in Mirth Connect that could allow unauthorized access and patient data manipulation. 574 units are affected and distributed nationwide.
CareFusion recalls approximately 10,460 Alaris PCA Module Model 8120 infusion pumps worldwide due to potentially bent female IUI connectors that may prevent proper device operation and delay treatment initiation.