State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Turtle Top is recalling 2013 Odyssey XL transit buses because a suspension fluid tank bracket may fail, causing the tank to separate and create a road hazard.
General Motors is recalling 2015 Chevrolet Corvette vehicles because the driver air bag module back plate may fracture, allowing the air bag to separate from the steering wheel.
Navistar is recalling 782 model year 2015 IC Bus CE school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Toyota is recalling 2014 Avalon, Camry, Sienna, Highlander, and 2015 Lexus RX350 vehicles because fuel may leak from a delivery pipe, increasing fire risk.
Navistar is recalling 2015 International Durastar and IC Bus CE vehicles because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Siemens is recalling about 9,000 SBGA-34 audible fire alarm bases because they may fail to sound an alarm, posing a risk of personal injury and property damage.
Chrysler is recalling 2008 Chrysler 300, Dodge Charger, Dodge Magnum, Jeep Commander, and Jeep Grand Cherokee vehicles because the ignition key may stick, potentially causing the engine to turn off while driving.
Wright Medical Technology is recalling 50 units of CLAW II Straight Plates because they were manufactured from an incorrect raw material.
Daimler Trucks is recalling 6,759 model year 2015 Freightliner, FCCC, Thomas Built Buses, and Western Star vehicles because a fuel filter component may separate, causing the engine to stall without warning.
General Motors is recalling 2015 Chevrolet Corvettes because a parking brake cable may not be fully seated, causing the vehicle to roll away on steep gradients.
Van Hool is recalling 2011-2013 TD925 buses because the front steering knuckle carrier may crack, potentially causing a wheel to separate and increasing crash risk.
Baxter Healthcare is recalling 157,080 containers of 0.9% Sodium Chloride Injection due to complaints of mold in the overpouch, raising concerns about sterility.
Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.
Illumina Inc is recalling 35 units of Illumina Worklist Manager software v1.0.15 because it fails to perform as intended.
Wright Medical Technology is recalling 497 CLAW II 2 Hole Plate OrthoLoc 3DSi orthopedic plates because they were manufactured from an incorrect raw material.
Wright Medical Technology is recalling 66 units of CLAW II Straight Plate OrthoLoc 3DSi orthopedic devices because they were manufactured from an incorrect raw material.
Wright Medical Technology is recalling 400 CLAW II 2 Hole Plate Ortholoc 3DSi units because they were manufactured from an incorrect raw material.
Ethicon Endo-Surgery Inc is recalling PROXIMATE skin staplers because a non-conforming component may cause the device to fire an unformed staple.
Wright Medical Technology is recalling 178 CLAW II 2 Hole Plate Ortholoc 3DSi units because they were manufactured from an incorrect raw material.
Pioneer Surgical Technology is recalling nine Streamline MIS Spinal Fixation System Fixed Rod Holders because they failed to lock onto the spinal rod.
Wright Medical Technology is recalling specific orthopedic claw plates because they were manufactured from an incorrect raw material.
Radiometer America Inc. is voluntarily recalling RADIANCE software versions 2.4X, 2.5X, and 2.6X. The recall is classified as Class II by the FDA.
Wright Medical Technology is recalling 9 units of CLAW 3.5mm plates because they were manufactured from an incorrect raw material.
Life Force of Tampa, LLC is recalling 10 Life Force Chambers because the product is marketed as a medical device without FDA premarket approval.
Wright Medical Technology is recalling 18 units of CLAW II Straight Plate OrthoLoc 3DSi orthopedic plates because they were manufactured from an incorrect raw material.