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.
Winnebago is recalling 2016-2017 Travato recreational vehicles because the liquid propane hose may contact the emergency brake cable, potentially causing a propane leak that increases the risk of fire or explosion.
Autoliv is recalling AI2 Air Bag Initiators manufactured between June 2016 and November 2016 because an improper chemical mix may prevent air bags from deploying properly in a crash.
Roush CleanTech is recalling propane conversion kits for Ford F-250 trucks because worn fittings may cause a propane leak, increasing fire risk.
Altec is recalling 2015-2016 AH125, AH150, and HL125 aerial devices because rotation bearing fasteners may fail, posing a risk of injury or death.
Altec Industries is recalling 2016 DLB Digger Derrick vehicles because fasteners securing the outer rotation bearings may fail, potentially causing the boom to move unintentionally.
Isuzu is recalling 2015-2017 NPR HD, NPR XD, NQR, and NRR trucks because burrs on the frame crossmember may cause transmission mounting studs to break, increasing crash risk.
Aluminum Trailer Company is recalling 2017 ATC Quest trailers because the lift platform may disengage from the safety lock, posing an injury risk.
Keystone is recalling 2017 Dutchmen Coleman recreational trailers because the Federal Identification Tag lists incorrect tire and rim sizes, which could lead to improper equipment use.
Britax is recalling B-Agile and BOB Motion strollers because a damaged receiver mount can cause car seats to fall, posing a hazard to infants.
Hale Products Inc. is recalling Fire Pump Engagement Pressure Switches that may fail in extremely cold temperatures, potentially delaying water delivery during fires.
Volvo is recalling 2017 XC90, S90, and V90 Cross Country vehicles because side air bag bolts may break, causing improper deployment in a crash.
PACCAR is recalling 2015-2018 Kenworth and 2017-2018 Peterbilt trucks because plastic fuel tee fittings may leak fuel, increasing the risk of fire.
Blue Bird is recalling 2015-2018 Vision school buses because battery box brackets may crack, causing the box to detach and become a road hazard.
Prevost is recalling 2017 H3-45 and X3-45 motor coaches because incorrectly forged steering arm levers may crack and fail, increasing crash risk.
Carestream Health is recalling DRX-Revolution Mobile X-Ray Systems because a complaint alleged the unit could not be stopped when applying the brake, resulting in a crash into an elevator.
Blue Bird is recalling 2015-2018 Vision transit buses because battery box brackets may crack, causing the box to detach and create a road hazard.
Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.
Boston Scientific is recalling 4,500 EMBLEM S-ICD Programmer Model 3200 units due to a potential risk of radio frequency interference causing unintended commands during in-clinic sessions.
Physio-Control is recalling LIFEPAK 15 Monitor/Defibrillators with End-Tidal CO2 options because the CO2 reading may intermittently display an incorrect value of XXX.
Stryker Leibinger is recalling QUINTUBE Monitor Packs and SPG Bulb Drain Systems because non-sterile products were incorrectly labeled as sterile.
Merge Healthcare is recalling 182 Eye Station capture stations because they may fail to capture eye images as intended, posing a risk to patient health.
Physio-Control is recalling LIFEPAK 12 Defibrillators because the End-Tidal CO2 reading may intermittently display an invalid value of XXX during operation.
Stryker Leibinger is recalling specific non-sterile Medpor implant sizer sets because they were incorrectly labeled as sterile. The recall covers 619 units distributed in the US and several international countries.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially leading to abnormal assay results.
Siemens is recalling specific lots of Dimension Vista Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially resulting in abnormal assay results.