State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DLT, LLC is recalling CravenSpeed Fiat Short Shifter shafts for 2011-2019 Fiat 500 vehicles because improper manufacturing may cause the shaft to break, increasing crash risk.
Nature's Truth is recalling wintergreen essential oil because the bottles do not meet child-resistant closure requirements, posing a poisoning risk to young children.
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Medtronic is recalling 15 Hancock II T510 Mitral Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Medtronic is recalling 15 Hancock II T510 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to cleaning procedure failures that may have caused cross-contamination.
Medtronic is recalling 15 Mosaic 310 Bioprosthesis mitral valves because they were mislabeled with incorrect sizes. The actual valves are larger than indicated on the packaging.
Qiagen is recalling 31 units of the RNeasy DSP FFPE Kit because a contaminant in the deparaffinization solution reduces RNA purification efficiency.
Medtronic is recalling 15 Mosaic 310 Bioprosthesis mitral valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
Tecan US, Inc. is recalling 40 Freedom EVO 200 laboratory robots because gas springs were not always replaced within the specified interval.
Medtronic is recalling 15 Hancock II T510 Bioprosthesis valves because they were mislabeled with an incorrect size. The actual valves are larger than indicated on the packaging.
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and possible cross-contamination from cleaning failures.
GE Healthcare is recalling ECG trunk cables that may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.
Altec is recalling 2018-2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, increasing the risk of injury or death.
Volvo Trucks is recalling 2019-2020 VAH, VHD, VNL, and VNR vehicles because over-tightened transmission air tank straps may deform and detach, creating a road hazard.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because rear side windows may be single-pane instead of laminated safety glass.
Volvo Trucks is recalling 2018-2020 VAH, VHD, VNL, and VNR models because a fuse may blow, preventing the transmission from shifting and increasing crash risk.
SRAM is recalling RockShox Lyrik and Yari front suspension forks because the lower leg assembly can break, causing riders to lose control and crash.
Nova Bus is recalling 2014-2017 LFS and LFS Artic buses because improperly tightened seat hardware may cause cantilever seats to drop, increasing injury risk.
Faraday is recalling about 4,450 electric bicycles because the seat posts can break, posing a fall hazard to riders.
Forest River is recalling 2019 Rockport work trucks with optional trailer brake controllers due to improper wiring that may prevent trailer brakes from activating.
Thor Motor Coach is recalling 1,554 motorhomes because a software defect may cause slide-out rooms to move unexpectedly, increasing injury risk.
Toyota is recalling 2017-2019 Camry, Corolla, RAV4, Sienna, and Yaris iA vehicles because an incorrect load capacity label may lead to unintentional overloading.
Yamaha is recalling about 1,500 Grizzly ATVs and Wolverine X2 ROVs because the owner's manuals contain information for the wrong models.
Honda is recalling specific 2005-2015 Acura and Honda vehicles because driver frontal air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.