State
73,741 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,780 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 2,942 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mayne Pharma is recalling specific bottles of Carbidopa and Levodopa Tablets because a foreign tablet was found in a bottle.
Braemar Manufacturing is recalling DL900 Holter Monitors because a software issue prevents new patient studies from starting. Existing recordings can still be downloaded.
The Binding Site Group is recalling 462 VaccZyme assay kits due to performance deterioration that may cause falsely elevated antibody results.
The Harvard Drug Group is recalling 330 cartons of Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
Integra LifeSciences is recalling 55 units of NeuraGen Nerve Guides because nonconforming product was mistakenly released for commercial use.
Lupin Pharmaceuticals is recalling specific lots of Bekyree oral contraceptives because they failed content and blend uniformity tests.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.
Yokohama is recalling specific commercial tires where the tread or bead may detach, potentially causing loss of vehicle control.
Thor Motor Coach is recalling 2020 SEQUENCE motorhomes because the transmission shifter cable may separate from the transmission, potentially causing unintended vehicle movement and increased crash risk.
Triumph is recalling 2013-2017 Trophy SE A1 motorcycles because improper brake hose routing may damage ignition wiring, causing engine stalls or lighting loss.
Volkswagen Group of America is recalling 2017-2019 Audi Q7 and 2019 Q8 vehicles because a steering shaft bolt may loosen, potentially causing a loss of steering control.
Eldorado National-Kansas is recalling 2017-2019 World Trans vehicles because seat belts may not be properly secured to the side wall, increasing injury risk in a crash.
Tornel is recalling specific Deportiva tires where adhesive failure may cause tread separation, increasing the risk of vehicle control loss and crashes.
Nissan is recalling 2020 Infiniti Q60 vehicles because the rear seat belt locking mechanism may fail to lock properly, increasing injury risk in crashes.
General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch wires may fracture, allowing the hood to open while driving.
BMW is recalling specific 2019-2020 motorcycles because the brake light may flash instead of staying steady during emergency braking, which can confuse other drivers.
Homestar is recalling Finch three-drawer dressers because they can tip over or entrap children if not anchored to the wall.
Jaguar Land Rover is recalling 2017-2018 Discovery vehicles because trailer lights may not function when towing with Daytime Running Lights on, increasing crash risk.
Volvo is recalling 2019-2020 S60, S90, V60, V90, XC40, XC60, and XC90 vehicles because a software issue may prevent the automatic emergency braking system from engaging.
Yamaha is recalling Line 6 Relay G10 wireless guitar systems because the lithium-ion battery can overheat and the cover can separate, posing fire and injury risks.
Kichler Lighting is recalling 52-inch LED ceiling fans because the arms holding the blades can detach, posing an injury risk. No injuries have been reported.
Axia Pharmaceutical is recalling Methylprednisolone Acetate/Bupivacaine Injectable Suspension due to a lack of assurance of sterility.