State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kia is recalling 2017 Sorento vehicles with 3.3L engines because the crankshaft may fail, increasing the risk of a crash or fire.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses Saf-T-Liner HDX and C2 school buses because a reinforcement bracket may be missing from seats with 3-point seat belts.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses Saf-T-Liner HDX and C2 models because a missing reinforcement bracket may compromise seat security during a crash.
Renthal is recalling Gen 1 and Gen 2 motorcycle clip-on handlebars because the clamp can crack and fail, posing a crash hazard. No injuries have been reported.
Bestherbs Coffee LLC is recalling New Kopi Jantan coffee packets because they contain undeclared desmethyl carbodenafil and milk.
Chiavna Saffron LLC is recalling Super Panther 7K Capsules because FDA analysis found the product was tainted with sildendafil and tadalafil and marketed without an approved NDA/ANDA.
Bella Pharmaceuticals is recalling Lidocaine Ophthalmic Gel 3.5% because the product lacks assurance of sterility.
Bella Pharmaceuticals is recalling Methylcobalamin 10mg vials because the company cannot ensure the product is sterile.
Bella Pharmaceuticals is recalling 6 bottles of Phenylephrine 2.5%/Tropicamide 1% Ophthalmic Solution due to a lack of assurance of sterility.
The Harvard Drug Group is voluntarily recalling Rugby Polyvitamin Liquid with Iron due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
The Harvard Drug Group is voluntarily recalling Major CertaVite Liquid due to possible B. cepacia contamination, which poses a risk of serious infection to patients with compromised immune systems or chronic lung conditions.
Navistar is recalling 2016 International and IC Bus vehicles because a steering axle nut may not be properly torqued, risking loss of steering.
Hyundai is recalling 2018 Santa Fe Sport vehicles because improperly manufactured front coil springs may fracture, potentially puncturing tires and causing loss of control.
Bella Pharmaceuticals is recalling G.A.C 25/100/250mg vials because the company cannot ensure the product is sterile.
The Harvard Drug Group is voluntarily recalling Major D-Vita Drops due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
Navistar is recalling 2018-2019 IC Bus CE school buses because the hydraulic brake hose may contact the tire, potentially causing fluid leaks and reduced braking performance.
The Harvard Drug Group is voluntarily recalling Rugby Liquid Vitamin C Supplement due to possible contamination with B. cepacia, which may cause serious infections.
Hyundai is recalling 2017 Santa Fe vehicles with 3.3L engines because crankshaft surface irregularities may cause engine bearing wear and vehicle stalling.
Rosenbauer is recalling one 2017 Commander emergency vehicle because a fuel pump gear may slip, causing sudden engine stall and crash risk.
Centurion Labs is recalling Ninjacof oral solution due to potential B. cepacia contamination. Consumers should stop using the product and return it to the pharmacy.
Bella Pharmaceuticals is recalling 644 vials of Fluorescein Sodium due to a lack of assurance of sterility. The affected lot was distributed nationwide.
Bella Pharmaceuticals is recalling MIC 25/50/50 vials because the company cannot ensure the product is sterile. The recall affects 5 vials distributed nationwide.
Bella Pharmaceuticals is recalling 82 vials of PF-Glutathione 200mg/ml because the product lacks assurance of sterility.
Leader Liquid Multivitamin Supplement for Infants and Toddlers is being voluntarily recalled due to possible contamination with B. cepacia, which can cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Major Tri-Vita Drops due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.