State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kawasaki is recalling 2019 Z900 ABS motorcycles because debris in the ABS hydraulic unit may cause wheel lockup during braking, increasing crash risk.
Hickory Springs is recalling FB11-39 DRW restraining barriers because they may fail to restrain unbelted occupants during a crash, increasing injury risk.
Forest River is recalling 2019 Cherokee recreational trailers because the Federal Placards list incorrect tire size information, which may lead to the installation of insufficient tires.
Isuzu is recalling 2019 NPR and Chevrolet 4500/5500 trucks because the odometer may display kilometers instead of miles, potentially delaying critical maintenance.
Forest River is recalling 2018-2019 Rockwood and Flagstaff recreational trailers because bunk bed door latches may fail, allowing the door to open while moving.
General Motors is recalling 2016-2018 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks because a fuel sensor defect may cause the front tank to overfill, potentially leading to a fuel leak and fire.
Daimler Trucks is recalling 2018-2020 Freightliner Cascadia trucks because the driver's frontal air bag may deploy unexpectedly, increasing crash risk.
Delta Electronics is recalling Eltek THEIA HE-t solar inverters because failing capacitors can cause heat buildup and cover ejection, posing fire and impact risks.
KTM is recalling 2015-2016 1290 Super Adventure motorcycles because fuel may leak from the tank cover, increasing fire risk.
General Motors is recalling specific 2016-2018 Cadillac and Chevrolet vehicles because the electric power steering system may fail, increasing crash risk.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable limits.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.
Prinston Pharmaceutical Inc is recalling Irbesartan and Hydrochlorothiazide tablets because FDA labs found the impurity NDEA above acceptable levels.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found N-nitrosodimethylamine (NDEA) above the acceptable daily intake level.
Aisin World Corp. of America is recalling Transmission Control Modules for 2016-2019 Mazda Miata MX-5 and 2017-2019 Fiat 124 vehicles. Incorrect programming may cause unexpected downshifting and abrupt deceleration.
Prinston Pharmaceutical Inc. is recalling Irbesartan 300 mg tablets because FDA testing found N-nitrosodimethylamine (NDEA) levels above the interim acceptable daily intake.
Subaru is recalling 2019 Forester and Crosstrek vehicles because a steering connector may short circuit, causing a loss of power steering assistance.
Roche Diagnostics is recalling Anti-HAV IgM test systems due to potential erroneous result messages on the cobas e 602 module.
Medtronic is recalling 1,100 Reservoir Y Adapters because the Y-connectors may tear or crack, potentially causing blood loss and circuit breaches during autotransfusion.
Sun Pharmaceutical is recalling BromSite (bromfenac) 0.075% ophthalmic solution due to a lack of sterility assurance. The recall affects 69,840 bottles distributed nationwide.
Haemonetics is recalling 4,576 Cell Saver Elite Processing Kits because the 70ml centrifuge bowl may leak during cell salvage processing.
Medtronic is recalling 7,587 Suction and Anticoagulation Assemblies because Y-connectors may tear or crack, potentially causing leaks and blood loss.
Siemens Healthcare Diagnostics is recalling 217 Atellica IM 1300 Analyzers worldwide due to multiple issues identified in software version 1.14.2 and lower.
Siemens Healthcare Diagnostics is recalling Atellica analyzer software versions 1.14.2 and lower due to multiple identified issues affecting in vitro diagnostic testing.
Dell is recalling hybrid power adapters sold with power banks because the casing can break, exposing internal metal components and posing an electric shock hazard.