State
73,584 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,925 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 2,925 recalls whose distribution notice names North Dakota specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Certain 2019-2021 Autocar Xpeditor and 2021-2022 Legend vehicles with a 7-inch display may experience restarts that hide critical warning lights. Dealers will replace the display free of charge.
Newmar is recalling 2020-2022 motorhomes due to steering gear mounting bolts that may back out, potentially causing loss of steering control. Owners should contact Newmar for a free replacement of affected bolts.
BMW is recalling certain 2021 X5 sDrive40i and X5 xDrive40i vehicles because the right front brake disc may have incorrect fasteners that could loosen over time, affecting vehicle control and increasing crash risk.
Mazda is recalling certain 2020-2021 CX-30 vehicles because the power liftgate may partially lower unexpectedly when parked on uphill slopes, risking injury to those accessing the rear storage area.
Ford is recalling 2020 F-350 SD trucks because incorrect labels may lead to overloading. Dealers will replace the labels free of charge.
Bendix is recalling SC-3 Single Check Valves because a loose retainer can cause air leaks in the brake system, increasing crash risk.
BMW is recalling 2020-2021 228i and M235i vehicles because the sunroof may continue closing after the vehicle is shut off, increasing injury risk.
Great Dane is recalling 2021-2022 Champion and 2022 Everest trailers because anti-lock brake sensor cables may be plugged into the wrong ports, increasing crash risk.
Autocar is recalling certain 2018-2021 Xpeditor vehicles because the turbocharger heat shield may fail and detach, creating a road hazard. Dealers will replace the component free of charge.
Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect concentration markings, posing a risk of dosing errors.
Argon Medical Devices is recalling 483 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect strength markings.
Ford is recalling 2004-2006 Ranger vehicles because certain replacement air bag inflators may explode during deployment, potentially causing serious injury or death.
Wahl Clipper Corp is recalling 161 units of the WAHL 4212 Heated Massager because the connection between the massager and heat element can overheat, posing a fire hazard.
Argon Medical Devices is recalling 863 TLAB Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.
Cummins is recalling certain Westport B6.7N natural gas engines because incorrect software calibration may prevent the engine from limiting speed or torque, potentially compromising safety functions like braking and stability control.
Argon Medical Devices is recalling 1,759 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Argon Medical Devices is recalling 583 Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.
Argon Medical Devices is recalling the TLAB Transjugular Liver Biopsy System because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Stanley Specialty Pharmacy is recalling Lidocaine/Tetracaine ointment because the lidocaine concentration is higher than listed on the label.
Argon Medical Devices is recalling 247 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.
Aomori Olympus is recalling SD-240U-25 electrosurgical snares because inspection found some sterile packages have inadequate seals, posing an infection risk.
Newmar is recalling 2017–2021 Dutch Star and 2021 Kountry Star motorhomes because the brake light switch may chafe against the windshield wiper mechanism, preventing brake lights from illuminating. This increases crash risk.
Ducati is recalling 2016-2018 XDiavel motorcycles because the side stand bracket may fail, causing the bike to fall and potentially injure nearby persons.
Aomori Olympus is recalling ForceMax Up injectors because some sterile packages have inadequate seals, posing a risk of infection if non-sterile equipment is used.