State
73,741 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling four 2017 vehicles due to improperly welded steering pins that may disable power assist, increasing crash risk.
Chrysler is recalling 2011-2014 Dodge Durango and Jeep Grand Cherokee vehicles to verify that previously installed brake booster shields were installed correctly to prevent reduced braking ability.
Curt Manufacturing is recalling Class 1 trailer hitches for 2016-2018 Mini Clubman and Countryman vehicles because the mounting points may be inadequate, causing the hitch to sag or separate.
Nissan is recalling 2017 Infiniti Q50 and Q50 Hybrid vehicles because the driver's air bag inflator may be improperly welded, increasing injury risk in a crash.
America New York RI Wang Food Group is recalling pork sausage products containing undeclared milk. The recall covers approximately 53,973 pounds distributed in New Jersey and New York.
Forest River is recalling 2015-2018 Vibe and 2016-2018 Rainier recreational trailers because the liquid propane line may have insufficient clearance, posing a fire risk.
Southwire is recalling Moonrays mystic globe and snow globe stake lights because light refraction can singe or melt nearby items, posing a fire hazard.
Mitsubishi is recalling 2004-2006 Lancer and 2004 Lancer Sportback vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Volvo Bus is recalling 2017-2018 Prevost 9700 transit buses because the accelerator pedal may not react when pushed, increasing crash risk.
Diono is recalling specific Radian, Olympia, Pacifica, and Rainier car seats manufactured between late 2013 and early 2017. The seats may not adequately protect children from chest injuries in crashes if installed forward-facing with only a lap belt.
Pierce Manufacturing is recalling 2015-2016 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a steering axle nut may not be properly torqued, risking loss of steering.
Kimble Mixer is recalling one 2014 Mixer Custom Chassis because improperly torqued hex nuts on the drive axle could cause the driveshaft to disconnect, increasing crash risk.
General Motors is recalling 2017-2018 Chevrolet Silverado and GMC Sierra trucks because front seat belt retractors may not perform correctly in a crash.
Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because door striker bolts may fail under load, potentially allowing doors to open in a crash.
Maquet Datascope is recalling 14,547 CS 100i Intra-Aortic Balloon Pumps because fluid ingress and false alarms could prevent therapy.
Madhava Honey Ltd is recalling its Chocolate Chip Cookie Mix because it may contain undeclared milk, posing a risk to individuals with milk allergies.
Cruiser RV is recalling 2018 Shadow Cruiser Ultra Lite trailers because rear axles were installed backwards, potentially reducing braking ability or causing brakes to lock up.
Maquet Datascope is recalling 14,547 CS 100 Intra-Aortic Balloon Pumps worldwide due to a defect that could prevent therapy initiation or continuation.
ImprimisRx is recalling Curcumin Emulsion 10mg/ml Injection vials because non-pharmaceutical grade PEG 40 Castor Oil was used due to supplier mislabeling.
Target is recalling approximately 175,000 Room Essentials 4-drawer dressers due to tip-over and entrapment hazards that can result in death or injuries to children.
Maquet Datascope is recalling CS 300 Intra-Aortic Balloon Pumps because fluid ingress could damage electronic boards, potentially preventing therapy initiation or continuation.
Elekta is recalling the MOSAIQ Medical Charged-Particle Radiation Therapy System because a software error inverts vertical table shifts, potentially directing therapy to incorrect areas.
ImprimisRx is recalling compounded Timolol ophthalmic drops because they were made with non-pharmaceutical grade PEG 40 Castor Oil due to supplier mislabeling.
Beckman Coulter is recalling LH 750, LH 780, and LH 500 analyzers because they may fail to flag blasts in some blood samples.
Cardinal Health is recalling Presource surgical kits because they contained BD SafetyGlide needles with loose polypropylene particulate in the fluid path.