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.
Heritage Pharmaceuticals is recalling specific lots of Gliptizide and Metformin HCL tablets because they failed impurity specifications. The affected bottles were distributed nationwide.
Mylan Pharmaceuticals is recalling specific lots of Fexofenadine HCl 60 mg tablets because they failed impurity specifications. The recall covers 13,856 bottles distributed nationwide.
Qualitest Pharmaceuticals is recalling Promethazine VC with Codeine Syrup because a stability lot failed impurity specifications.
Gillig is recalling 623 Low Floor transit buses from 2013-2015 because brake hoses may rub against suspension towers, potentially causing air leaks and increased stopping distances.
Beech-Nut Nutrition is recalling approximately 1,920 pounds of Stage 2 sweet potato and chicken baby food jars due to possible glass contamination.
Yamaha is recalling 350 model year 2015 YZFR1M motorcycles because a rear shock absorber nut may loosen, potentially causing loss of vehicle control.
Fontaine Modification is recalling 2006-2015 Freightliner M2 trucks with dual steering because brake lights may not illuminate if the primary air supply is depleted.
San Pedro Manufacturing is recalling about 4,800 renovated mattresses and foundations because they fail to meet federal fire safety standards.
Yamaha is recalling about 3,500 Viking VI side x side vehicles because rear wheels can loosen, causing the vehicle to crash.
Leader Slaughterhouse, LLC is recalling approximately 1,800 pounds of veal carcasses produced without the full benefit of federal inspection. The product was distributed to customers in Pennsylvania and New York.
Crossroads is recalling 2016 recreational trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
Hyundai is recalling 2015 Accent vehicles because the occupant detection system may fail to identify child restraints in cold weather, preventing front air bag deactivation.
Harley-Davidson is recalling 2015 XG500 and XG750 motorcycles because they may lack rear reflector assemblies, reducing visibility to other drivers.
Harley-Davidson is recalling 2014-2015 motorcycles because the clutch master cylinder may fail to disengage the clutch, increasing crash risk.
Land Rover is recalling 2015 LR4 vehicles because an ABS software error may disable stability and traction control systems, increasing crash risk.
Spartan Motors is recalling 66 model year 2015 K3 chassis because tag axle suspension hangers may move, causing the axle to shift off center and increasing crash risk.
Grand Design is recalling specific 2015-2016 Reflection and Solitude trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
Trans-Air is recalling 835 GM G3500 and G4500 vans modified with specific compressor kits due to a loose electrical connection that may cause a vehicle fire.
WhiteWave Foods is recalling Horizon Cheddar Sandwich Crackers because they may contain undeclared peanuts due to a packaging error.
Brinkhoff & Monoson Inc is recalling HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend because it may contain undeclared peanut allergens.
Baxter Healthcare is recalling 196,128 containers of 0.9% Sodium Chloride Injection due to lack of sterility assurance and leak complaints.
Baxter Healthcare is recalling 7,444 containers of Clinimix E 5/20 due to a lack of assurance of sterility and increased leak complaints.
Pega Medical Inc. is recalling 7 units of the 4.8mm GAP Nail because of failures at the distal cortical screw holes, primarily in patients with specific bone conditions.
Medtronic is recalling 6,040 Model 5392 temporary pacemakers because specific AA batteries may fail to connect, potentially stopping pacing therapy.
Maternal Science Inc. is recalling Healthy Mama Boost It Up Mighty Mango Protein Drink because it contains undeclared milk.