State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Samsung is recalling 2.8 million top-load washing machines because the top can detach during use, posing an impact injury risk.
PTIC is recalling 2014-2016 Stratos asphalt distributor trailers because fully loaded weight may exceed axle capacity, risking bearing overheating or hub detachment.
PACCAR is recalling 2017 Peterbilt and Kenworth trucks equipped with specific Goodyear tires that may partially separate, increasing crash risk.
Terex is recalling 2009-2014 TC and TCX hybrid electric trucks because improper wiring may cause the aerial boom to move unintentionally, increasing the risk of injury.
Yamaha is recalling 2,550 WR250R motorcycles because a cracked clutch oil seal may leak engine oil onto the rear tire, increasing the risk of a crash.
Meritor is recalling specific MX810 Series front drive steer axles because lower king-pins may fracture, potentially causing wheel end separation and loss of vehicle control.
E-One is recalling 2014-2016 Typhoon, Quest, and Cyclone fire trucks equipped with aerial ladders because a filter design change may cause hydraulic fluid leaks.
KTM North America is recalling about 1,200 model year 2017 KTM and Husqvarna off-road motorcycles because the front brake master cylinder can malfunction, posing a crash hazard.
St Jude Medical is recalling specific implantable defibrillators because a lithium cluster in the battery can cause a short circuit and premature depletion.
Roche is recalling cobas 8000 Modular Analyzers and e602 Immunoassay Analyzers after four reports of injury caused by a sharp edge on the sample rack tray.
Ortho-Clinical Diagnostics is recalling the enGen Laboratory Automation System because a software error may cause sample identification to be mismatched with assay results.
Roche is recalling 9,014 cobas p 312 Pre-Analytical System calculator/data processing modules due to four reported injuries caused by a sharp edge on the sample rack tray.
Roche is recalling 9,014 cobas p 701 Post-Analytical Units because a sharp edge on the sample rack tray caused four reported injuries.
Roche is recalling 9,014 cobas p 512 Pre-Analytical Instruments after four reports of injury caused by a sharp edge on the sample rack tray.
Roche is recalling 9,014 cobas 8000 Sorting System calculator/data processing modules after four reports of injury caused by a sharp edge on the sample rack tray.
Roche is recalling 9,014 cobas p 501 Post-Analytical Units because a sharp edge on the sample rack tray caused four reported injuries.
McCormick is recalling Club Size Original Taco Seasoning Mix due to undeclared milk. The recall covers 14,570 containers distributed nationwide.
Roche is recalling cobas 6000 Series analyzers because the sharp edge of the sample rack tray center guide rail caused four reported injuries.
St Jude Medical is recalling implantable cardiac defibrillators and cardiac resynchronization therapy defibrillators due to a battery defect that can cause premature depletion.
Isuzu is recalling 2014-2016 NPR, NPR HD, and 2016 Chevrolet Low Cab Forward 3500/4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.
St Jude Medical is recalling specific implantable cardiac defibrillators and cardiac resynchronization therapy defibrillators because a lithium cluster in the battery can cause a short circuit and premature battery depletion.
Roche is recalling 9,014 cobas p 471 centrifuge units because a sharp edge on the sample rack tray caused four reported injuries.
Roche is recalling URISYS 2400 Urine Analyzers because a sharp edge on the sample rack tray caused four reported injuries.
Roche is recalling Modular Pre Analytics EVO/Plus systems because a sharp edge on the sample rack tray caused four reported injuries.
Roche is recalling COBAS INTEGRA 800 analyzers after four reports of injury caused by the sharp edge of the sample rack tray.