State
73,824 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.
Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling specific 2011-2014 Dodge, Chrysler, and Jeep vehicles because the alternator may fail, causing the vehicle to stall or catch fire.
General Motors is recalling 40,683 vehicles from 2014-2017 because a software error may prevent front air bags and seat belt pretensioners from deploying in a crash.
BMW is recalling 2014-2017 R1200GS and R1200GS Adventure motorcycles because the fixed fork tube may separate from the seal plug, increasing crash risk.
Adient is recalling specific Recaro commercial bus driver seats because the seat belt buckle may be stuck in the locked position, preventing the seat belt from latching.
Zero Motorcycles is recalling 2017 S, DSP, and SR models because the turn signal flasher may not alert the operator if a signal fails, increasing crash risk.
MORryde is recalling Jerry Can holders that may tear apart from the spare tire mount, creating a road hazard.
Chrysler is recalling 2017 Ram 1500 trucks because a broken fuel tank control valve may leak fuel if the vehicle is inverted, increasing fire risk in a rollover crash.
Chrysler is recalling 2017 Dodge Challengers with 5.7L V8 engines and eight-speed automatic transmissions because the vehicle may not stay in Park, increasing crash risk.
Chrysler is recalling 2011-2015 Dodge Journey vehicles because the driver's frontal air bag wiring may chafe and short circuit, causing unexpected deployment.
Chrysler is recalling 2017 Jeep Compass vehicles because the User's Guide contains reversed battery terminal polarity for jump starting, which may increase the risk of injury.
Forest River is recalling specific 2015-2018 transit buses and work trucks because a flexible coupling may fail, potentially damaging brake and fuel lines.
Ford is recalling 2017 Edge, Fusion, and Lincoln MKZ vehicles with 2.0L engines and six-speed automatics because torque converter weld studs may be inadequate, risking loss of vehicle movement.
Cub Cadet is recalling approximately 4,000 2016 Challenger utility vehicles because air in the brake system can cause brake failure, posing a crash hazard.
BMW is recalling 2006 3 and 5 Series vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.
Severn Peanut Co. is recalling Ava's brand Organic Cashews Roasted & Salted 8 oz. tubs because the product may be contaminated with Listeria monocytogenes.
Cummins is recalling L9 heavy-duty diesel engines installed in Pierce fire trucks because improperly tightened capscrews may cause the flexplate to separate, potentially leading to engine stalling and a crash.
Severn Peanut Co. is recalling specific lots of Avas Organic Roasted Unsalted Cashews due to potential Listeria monocytogenes contamination.
Home Depot is recalling Hampton Bay and Home Decorators Collection crystal chandeliers because halogen bulbs can melt parts, posing fire and burn risks.
DeRoyal Industries is recalling 426 Dolphin Inflation Devices due to a primary packaging defect that may compromise sterility.
Allergan is recalling 648 units of Blephamide ophthalmic ointment because stability testing showed impurities exceeding specifications.
Severn Peanut Co. is recalling Avas Organic Roasted Unsalted Almonds due to potential Listeria monocytogenes contamination. The product was distributed in New Jersey, New York, Pennsylvania, and Connecticut.
Olympus Corporation of the Americas is recalling 1,264 High Frequency Resection Electrodes because loop wires may break at the distal end.
Shimadzu Medical Systems is recalling ceiling-type X-ray tube supports because cracks may develop on the tube holding shaft, posing a risk of equipment failure.
Merge Healthcare is recalling 219 SpO2 connecting cables for its Hemodynamics monitors because they may stop displaying patient SpO2 readings, causing a slight delay in patient care.
Carestream Health Inc is recalling DRX-Revolution Mobile X-Ray Systems because missing screws could cause the tube and yoke assembly to separate.