State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Eldorado is recalling specific 2010-2016 bus models because missing welds on seat brackets could cause seat belts to detach during a crash.
KTM North America is recalling about 3,700 model year 2016 Husqvarna and KTM motocross motorcycles because the front wheel spoke assembly can fail, causing crashes.
IKEA is recalling LATTJO tongue drums and drumstick sets because rubber balls can detach, posing a choking hazard to children.
Steelcase is recalling about 17,000 Rocky model swivel chairs because screws can detach, posing a fall hazard. One injury was reported.
School Specialty is expanding a recall of NeoRok stools that can break during use, posing a fall hazard to children.
Altar'd State is recalling monogrammed coffee mugs because metallic paint accents can spark in the microwave, posing a fire hazard.
Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.
Skinny Latina LLC is recalling 18,822 bottles of Million Dollar Marinade due to undeclared soy. The product was sold at Target, Whole Foods, and Fresh Market.
Gillig is recalling 6,734 Low Floor transit buses from 2010-2015 because missing welds on seat brackets could cause seat belts to detach during a crash.
Pine Valley Foods is recalling specific batches of pre-portioned cookie dough because they contain undeclared milk or egg allergens.
Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.
ConAgra Foods is recalling David Trail Mix Sweet & Salty bags because they contain undeclared milk. The product was distributed nationwide and to specific foreign locations.
Boston Scientific is recalling ACUITY Pro Coronary Sinus Guide Catheters due to a potential for the proximal handle to separate from the shaft.
Pine Valley Foods is recalling pre-portioned sugar and walnut chocolate chunk cookie dough because they contain undeclared milk and egg, respectively.
Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.
Pine Valley Foods is recalling specific sugar cookie products due to undeclared milk and egg allergens.
Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.
Pine Valley Foods is recalling specific Hello Kitty sugar cookie kits because they contain undeclared milk and egg.
Biomet 3i is recalling 30,111 Protection Cap Kits worldwide due to inadequate biocompatibility testing. The devices are used as accessories for dental implants.
Corflex is recalling 1,406 post-operative knee braces because they may fail to maintain a locked position, potentially causing loss of balance or undesired knee movement.
Corflex is recalling 10 units of the Brielle Ortho Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.
Corflex is recalling 42 units of the Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.
Baxter Healthcare is recalling Y-Type Spike Adapters due to the potential presence of dark loose particulate matter on the spike.
Made In Nature is recalling Sriracha Chili Kale Chips due to undeclared soy allergen from Tamari. The recall covers 50,176 units distributed nationwide.
Biomet 3i is recalling specific dental impression copings due to inadequate biocompatibility testing. The devices are distributed worldwide, including in the US.