State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Livie and Luca is recalling Carta and Cotton children's shoes because a metal thread inside the liner can poke through and cut a child's foot.
Chrysler is recalling 2011 Dodge Durango and Jeep Grand Cherokee vehicles because a fuel pump relay may fail, causing the vehicle to stall without warning.
AmTRAN Video is recalling JVC 42-inch flat panel televisions because the stand neck can crack, causing the TV to tip over and pose an impact injury risk.
Allied Recreation Group is recalling 2015 Monaco Holiday Rambler fifth wheel trailers because incorrect Federal Certification labels may lead to improper tire inflation and increased crash risk.
FGX International is recalling about 215,000 children's sunglasses because the surface paint contains excessive levels of lead, which is prohibited under federal law.
Chrysler is recalling 2014 Ram ProMaster vans because head restraints may exceed safety limits, increasing injury risk in rear-end collisions.
Chrysler is recalling 2013-2015 Ram C/V Tradesman vans because road hazards may cause front air bags to deploy unexpectedly, increasing crash risk.
Abrams Royal Pharmacy is recalling 74 units of Mineral IV Injection found to contain Sphingomonas paucimobilis, indicating non-sterility.
Abrams Royal Pharmacy is recalling all unexpired sterile drug products due to a lack of assurance of sterility. The products were distributed nationwide and to Canada.
NHTSA is recalling 281 model year 2014 Collins and Mid Bus school buses because inadequate adhesive on interior side panel joints may fail to meet federal safety standards.
Beta Labs is recalling Phentylene capsules because they contain DMAA, a substance not permitted in dietary supplements.
Daimler Trucks North America is recalling 2014-2015 Western Star 4900 trucks manufactured without Anti-lock Brake Systems, which increases the risk of wheel lockup and crashes.
Beta Labs is recalling 743 units of PHEnFX dietary supplements because they contain DMAA, a substance not permitted in dietary supplements.
Ford is recalling 2005-2008 Escape and 2006-2008 Mariner hybrid vehicles because a coolant pump failure may cause the powertrain to shut down, increasing crash risk.
Great Innovations is recalling about 70,000 Ultrasonic Clean Mist Humidifiers sold by QVC because water can enter the base and cause a fire hazard.
Beta Labs is recalling Red Vipers dietary supplements because they contain DMAA, an ingredient not permitted in dietary supplements.
Alkermes is recalling 4,364 vials of VIVITROL (naltrexone) nationwide because customer complaints reported the product failed to deliver the dose.
Siemens is recalling 2,757 Dimension EXL Integrated Chemistry Systems because a reagent lid hinge may shift during maintenance, posing a risk of physical injury to operators.
Curbell Medical is recalling CareSense Wireless Advanced LCD Bed and Chair Monitors because a circuit board modification disabled the alarm function.
Orbea is recalling 715 Avant bicycles because the front fork can crack, posing a fall hazard. No injuries have been reported.
iDevices is recalling about 48,500 cooking thermometer probes in the U.S. and 510 in Canada because the internal plastic insulator can melt and fall into food.
Medtronic is recalling MiniMed Paradigm insulin pumps because users may have accidentally programmed them to deliver the maximum bolus amount.
Zimmer, Inc. is recalling 15 units of a specific knee prosthesis component because internal review found five raw material forgings with defects that were not segregated.
Thermedx LLC is recalling 21 units of the P4000 Fluid Management System because a manufacturing change to the canister ring may cause the deficit display to read higher than the actual fluid deficit.
Beta Labs is recalling Oxyphen XR fat burner capsules because they contain DMAA, a substance not permitted in dietary supplements.