State
73,824 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling 2017 Civic Hatchback and Type R vehicles because replacement seatback pads may block side air bags, increasing injury risk in a crash.
General Motors is recalling certain 2009-2018 Chevrolet, GMC, and Isuzu vehicles because the installed fire extinguishers may clog or detach, potentially failing to function during a fire.
Honda is recalling various 2001-2012 models because the front passenger air bag may have been installed incorrectly during replacement, increasing injury risk in a crash.
Nutrizone LLC is recalling all packages of Nirvanio Green Malay Kratom because dietary supplements have the potential to be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Nirvanio Bali Kratom because dietary supplements may be contaminated with Salmonella.
Blue Bird is recalling 2018-2019 All American and Vision transit buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.
Philips is recalling 19 Brilliance iCT SP CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Blue Bird is recalling 2018-2019 Vision and All American school buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.
Nutrizone LLC is recalling all packages of Pain Out Green Malay Kratom because dietary supplements can be contaminated with Salmonella.
Lupin Pharmaceuticals is voluntarily recalling 40,824 bottles of Cefdinir powder for oral suspension because the drug was found to be superpotent.
Nutrizone LLC is recalling all packages of Nirvanio Maeng Da Kratom because dietary supplements have the potential to be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Pain Out Thai Kratom because dietary supplements may be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Cali Green Malay Kratom because dietary supplements may be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Pain Out Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.
Nutrizone LLC is recalling all packages of Cali Thai Kratom because dietary supplements may be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Nirvanio Special Reserve Kratom because dietary supplements can be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Cali Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because ramp-securing bolts may loosen or break, increasing the risk of injury or a crash.
Divinity Product Distribution LLC is recalling kratom capsules because the ingredient lacks adequate safety information to ensure it does not present a significant risk of illness or injury.
Divinity Product Distribution LLC is recalling kratom powder products because the ingredient lacks sufficient safety data to ensure it does not pose a risk of illness or injury.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because missing hardware may allow the rear ramp to detach while moving, increasing crash risk.
Volkswagen is recalling 2018 Tiguan long wheelbase vehicles because a rear shock absorber loop may separate, potentially causing loss of vehicle control.
Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
Philips is recalling Panorama 1.0T MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.