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.
Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because the passenger air bag inflator may fail to ignite, preventing deployment in a crash.
King's Command Foods is recalling approximately 26,138 pounds of ground beef products due to possible contamination with extraneous materials, including metal objects.
Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.
Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.
Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.
Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.
Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.
RDG Global is recalling about 2,600 girls' hooded sweatshirts sold at Nordstrom because the hood drawstrings pose a strangulation hazard to children.
Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.
United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.
Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.
United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.
Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.
United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.
United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.
Volkswagen is recalling 2007-2010 Touareg vehicles because a fuel filter flange may crack and leak fuel, increasing the risk of fire.
Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.
Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.
Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.
Siemens is recalling specific Calibrator A Kits due to a negative bias in FT4 assays and potential calibration failures on certain systems.
Volkswagen Group of America is recalling 2017 Audi A5 and S5 Cabriolets because a seat belt pretensioner component may detach during a crash, creating a projectile hazard.
Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.
Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) 30 mg capsules because they failed to meet dissolution specifications.