State
73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.
Of the 12,955 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 3,701 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 116,160 vehicles because road salt may corrode steering bolts, causing loss of power steering assist and increasing crash risk.
Indian Motorcycle is recalling 2019 Chieftain models because tail lights may be too bright, potentially confusing other drivers and increasing crash risk.
Decathlon USA is recalling about 50 Rocky Screwgate carabiners because incorrect assembly can cause them to unlock while in use, posing a risk of serious injury or death.
Pearhead is recalling Ubbi Connecting Bath Toys because they can break and create sharp points, posing choking and laceration hazards to young children.
FCA US is recalling 2019 Ram 2500 and 3500 trucks because incorrect assembly fluid in brake calipers may cause seals to swell, leading to dragging brakes and increased crash risk.
Sandoz is recalling approximately 636,000 bottles of Losartan Potassium and Ezetimibe because the caps do not meet child-resistant requirements, posing a poisoning risk to children.
Rite Aid is recalling about 18,800 folding patio chairs because the frames can bend, causing users to fall and potentially get injured.
Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems due to reports of burst balloons that caused difficulty retrieving the device during procedures.
Dole Fresh Vegetables is recalling specific lots of Dole Baby Spinach after a Michigan state test detected Salmonella.
Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems because burst balloons can make it difficult to remove the device from patients.
SCA Pharmaceuticals is recalling 922 syringes of Ketamine 50 mg/5 mL injection due to a lack of assurance of sterility. The product was distributed nationwide.
Whirlpool is recalling about 26,300 glass cooktops with touch controls because the surface elements can turn on by themselves, posing burn and fire hazards.
Ford is recalling 639,137 vehicles because a missing part in the seat back recliner mechanism may reduce strength and fail to restrain occupants in a crash.
BMW is recalling 2020 MINI Cooper, Cooper S, and JCW vehicles because rear side trim panels may lack crash pads, increasing injury risk in side impacts.
Ford is recalling 2019 Fiesta vehicles because incorrect assembly fluid in brake calipers may cause seals to swell, leading to brake drag and overheating.
Jayco is recalling 2019 Embark motorhomes because insufficiently tightened steering shaft bolts may allow the steering column to come loose, increasing crash risk.
Jayco is recalling 2019-2020 Eagle HT fifth wheel trailers because incorrect pin box bolts may allow the box to rotate in two places, increasing crash risk.
Makzemo LLC is recalling BALQEES SPICES Yemeni Spices Mix because the product contains high levels of lead. The recall affects 600 units distributed in New York and Michigan.
Kirkland's is recalling about 3,000 chests of drawers because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards.
Entegra is recalling 2019-2020 motorhomes because steering shaft bolts may be loose, risking loss of steering control and crashes.
Yamaha is recalling about 16,000 golf cars and specialty vehicles because a USB power module can overheat and melt, posing a fire hazard.
BMW is recalling 2020 X5 and X7 vehicles because steering rack pinion teeth may break, causing loss of steering control and increasing crash risk.
Edwards Lifesciences is recalling 362 units of the SAPIEN 3 Ultra Transcatheter Heart Valve System due to reports of burst balloons that complicate device retrieval.
Pierce Manufacturing is recalling one 2019 Pierce Tanker vehicle because insufficient front axle lubrication may damage wheel end bearings, potentially causing wheel separation and loss of control.
Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems due to reports of burst balloons that caused significant difficulty retrieving the device during procedures.