State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pfizer is recalling 137 bottles of Oxecta (oxycodone HCl) 5 mg tablets because they failed impurity and degradation specifications.
Arrow International Inc. is recalling 165 units of FiberOptix Intra-Aortic Balloon Catheter Kits because the outer package label incorrectly identifies the product size.
AvKARE Inc. is voluntarily recalling 431 unit dose packs of Quinapril Tablets USP, 40 mg, because the medication was found to be subpotent.
AvKARE Inc. is voluntarily recalling 214 unit dose packs of Quinapril 5 mg tablets nationwide because the medication is subpotent.
Mercedes-Benz is recalling 2015 C300 and C400 vehicles because the fuel delivery module may be improperly secured or have pinched wires, increasing the risk of fire or stalling.
Meritor is recalling specific MT-40-14X rear drive train axles because low lubricant levels may cause bearing failure and increase crash risk.
Blue Bird is recalling 2013-2016 All American and Vision school buses because incorrect fasteners may cause seat belts to be improperly anchored, increasing injury risk in crashes.
Mercedes-Benz is recalling certain CLS 400, 550, and 63 models because LED tail lights may not illuminate on the sides, reducing rear visibility and increasing crash risk.
K.J. Sportswear is recalling about 9,200 children's Thor pajamas because they fail to meet federal flammability standards, posing a risk of burn injury.
Comet USA is recalling about 2,100 efco gas trimmers because the engine muffler can break during use, posing a fire hazard. Consumers should stop using the units and return them for a free replacement.
Toyota is recalling 2012-2015 Yaris vehicles sold in Puerto Rico because the roof headliner may not provide proper occupant protection in a crash.
Winnebago is recalling 2015 ERA, View, and Itasca Navion vehicles because an incorrectly installed door component may make doors harder to open after a crash.
Harbor Freight is recalling specific Haul Master trailer light kits because they may fail to meet federal safety standards, potentially reducing trailer visibility to other drivers.
Forest River is recalling 2015 XLR Nitro XLT31FQSL recreational vehicles because the fueling station hose may be too close to a fuel-burning appliance, increasing fire risk.
Tiffin Motorhomes is recalling 2014 Breeze motorhomes because a steering knuckle may fracture, potentially causing loss of vehicle control and increasing crash risk.
Haldex is recalling specific air brake actuators where an internal defect may cause brake drag and overheating, increasing the risk of fire.
Rapala is recalling StrikeMaster Lithium Lazer ice augers because the trigger switch may fail to turn off the unit, posing an injury risk.
Forest River is recalling one 2015 XLR Hyperlite trailer because fuel vapors may ignite near a fuel-burning appliance. The unit is being repaired at the dealership before delivery.
PACCAR is recalling 2006-2016 Peterbilt trucks because tire labels may list incorrect pressure, risking tire failure and crashes.
Multiprens is recalling STK-100 triangle kits manufactured between October 2011 and July 2014 because they fail to meet Federal Motor Vehicle Safety Standard No. 125.
Sugar Daddy LTD is recalling 1,000 Caramel Apples because CDC epidemiologists linked a Listeria monocytogenes illness outbreak to the product.
Sugar Daddy LTD is recalling caramel apples linked to a Listeria monocytogenes outbreak. Consumers should not eat the product.
Invacare is recalling 1,942 TDX, FDX, and Storm Series power wheelchairs because wire pinching can cause smoking, sparking, or fire.
HeartWare Inc is recalling 4,845 HeartWare Controllers used in ventricular assist systems because they are more susceptible to electrostatic discharge (ESD) than newer models.
Invacare is recalling 60 FDX, TDX, and Storm Series power wheelchairs because wire damage can cause smoking, sparking, or fire.