State
72,971 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,921 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 727 (25%) are Severe.
Which agencies issued them
These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2025 Bronco four-door vehicles because the left-hand rear door may open from inside when the child safety lock is engaged, increasing injury risk.
Ford is recalling certain 2020-2025 Explorer and Lincoln Aviator vehicles because the easy-entry second-row seat switch may bind, letting seats unlatch, fold or slide unexpectedly.
Endless Pools is recalling about 11,500 Manual Retractable Security Pool Covers because improper installation can leave gaps larger than 4.5 inches, posing drowning and entrapment risks to children.
Mammut Sports Group is recalling Skywalker Pro Via Ferrata Sets because the carabiner can open without engaging the safety latch, creating a risk of serious injury or death from falls.
Starway International Group is recalling approximately 9,513 pounds of frozen fish balls imported from Vietnam because the producing establishment is not eligible to export to the US.
Honda is recalling certain Acura TLX, Acura MDX and Honda Pilot vehicles because the brake pedal pivot pin was not secured properly, which can shift the pedal out of position.
GM is recalling certain 2019-2024 Chevrolet Silverado Medium Duty trucks because the brake pressure sensor may leak fluid into the switch and short circuit. Owners are told to park outside.
Approximately 1,158,000 Anker PowerCore 10000 power banks (model A1263) are recalled because their lithium-ion batteries can overheat, creating fire and burn hazards. Anker has received 19 reports of fires and explosions, including property damage totaling over $60,700.
Bugaboo North America is recalling about 18,280 Giraffe highchairs because the legs can detach from the frame if screws are not properly tightened during assembly, posing a risk of serious injury or death. The company has received 22 reports of leg detachment, including 13 reports of minor injuries.
Volvo is recalling certain electric and plug-in hybrid models because the vehicle may lose brake function while coasting downhill in "B" mode or One Pedal Drive. Owners are told not to use those modes until repaired.
Agro Superior Group is recalling about 16,530 Oliver & Smith 6-inch mattresses sold online because they violate federal flammability standards and pose a risk of serious injury or death from fire. Consumers should stop using them immediately.
Harley-Davidson is recalling 2018-2024 Softail motorcycles because a rear shock absorber component may break and damage the tire, increasing crash risk.
Chrysler is recalling certain 2023 Pacifica and Voyager vehicles because a manufacturing error may prevent the rearview camera image displaying, failing FMVSS 111.
Chrysler is recalling certain 2024-2025 Dodge Charger vehicles because the amplifier may be missing software, preventing exterior sound including pedestrian warnings.
TI Outdoor Power Equipment is recalling about 113,000 RYOBI 40V 24-inch cordless hedge trimmers because the blade can unexpectedly activate from pressing only one control, causing lacerations. Consumers should stop using the trimmer and return it for a free replacement.
SunMed Holdings is recalling 11,358 Adult Manual Resuscitators because the filter may be incorrectly attached to the patient port instead of the exhalation port, risking interruption or delay in patient resuscitation that could cause serious harm or death.
Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.
Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.
Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.
Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.
Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.
GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.
Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.