State
73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Bird is recalling 2018-2021 Vision and All American school buses because the electric drive train may fail to detect high-voltage isolation faults, posing a shock risk to service personnel.
USDA FSIS issued a public health alert for raw ground turkey products from Plainville Brands, LLC, linked to a multistate Salmonella Hadar outbreak.
Spartan Fire is recalling 2019-2021 Gladiator and MetroStar vehicles because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist.
BorgWarner is recalling specific Ford and GM start/stop accumulators because missing or loose bolts may cause oil leaks, increasing the risk of transmission failure or fire.
Yamaha is recalling 2015-2020 XC155 scooters because a primary sheave nut may loosen and fall off, potentially causing the engine to stall and increasing crash risk.
Keystone is recalling certain 2020-2021 Bullet trailers with defective bedroom emergency egress windows. An incorrect crank handle may make the window difficult to open in an emergency.
Honda is recalling 2021 CBR1000RR-R Fireblade SP motorcycles because incorrectly installed rear cushion connecting plates may break, causing a sudden drop in vehicle height and increasing crash risk.
Verizon is recalling 2.5 million Ellipsis Jetpack mobile hotspots because the lithium-ion battery can overheat, posing fire and burn hazards.
Meritor is recalling specific TSE T2024 Air Brake Chambers because incorrect springs may cause the pressure plate to shift, potentially leading to a loss of air pressure and increased crash risk.
Jaguar is recalling 2017-2018 and 2020 XE vehicles because missing spot welds may weaken the rear rail assembly, increasing the risk of a crash during towing.
General Motors is recalling specific Buick, Chevrolet, and GMC SUVs because side curtain air bags may not be properly attached, increasing injury risk.
General Motors is recalling specific 2014-2016 Chevrolet and GMC vehicles because a driver's seat belt cable may break, reducing safety protection.
Geo Essential LLC is recalling Wintergreen and Alleviate essential oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Keystone RV Company is recalling 2020-2021 Dutchmen Aspen Trail trailers because improperly installed ramp door fasteners may strip, potentially detaching the rear door and increasing injury risk.
Wilton Industries Inc. is voluntarily recalling 1,638 units of Valentine Chip Crunch Sprinkles nationwide due to undeclared milk.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Holiday Home Assorted Treat Toppings nationwide due to undeclared milk, a major allergen.
FDA recalls CF Delivery Dev Caps Bravo x5 capsules because they may fail to attach to the esophagus, leading to aspiration.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets because a toxicological assessment found potential for aluminum ions to leach into warmed fluids.
Medtronic is recalling specific Evera and Visia ICD models because a small percentage may experience a shortened Recommended Replacement Time to End of Service interval.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
The FDA is recalling Bravo pH Capsule Delivery Devices because the capsule may fail to attach to the esophagus, leading to aspiration and potential hospitalization.
Goal Zero is recalling about 7,850 EC8 power cables because the connector pins can deform and overheat, posing a fire hazard. Four reports of overheating or fire have been received, with no injuries.