State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Polaris is recalling about 3,900 Ranger EV recreational off-highway vehicles due to a wiring defect that can cause unexpected acceleration and crashes.
Honda is recalling specific 2018 and 2019 motorcycles because a transmission part may detach, causing gear misalignment that increases crash risk.
Braun is recalling 2014-2019 Toyota Sienna mobility van conversions because incorrect brake line fittings may cause a loss of rear braking power.
Generation Brands is recalling Small Stratton glass pendant light fixtures because they can detach from the cord and fall, posing an injury risk.
Polaris is recalling about 1,200 Model Year 2019 RZR XP 4 Turbo S recreational off-highway vehicles because the brakes can fail, posing crash and injury hazards.
Perdue Foods is recalling approximately 31,703 pounds of ready-to-eat chicken products that may contain pieces of bone material.
Karma Automotive is recalling 295 2018 Karma Revero vehicles because the upper intrusion bar in the front left door may be split, reducing side-impact protection.
Chrysler is recalling 2019-2020 Ram 1500 vehicles because a software defect may disable air bags and seat belt pretensioners, increasing crash injury risk.
Johnsonville is recalling ready-to-eat jalapeno cheddar smoked sausage links due to possible hard green plastic contamination. No adverse reactions have been reported.
Jayco is recalling 2020 Greyhawk motorhomes because a defective brake relay valve may cause extended stopping distances, increasing crash risk.
Mazda is recalling 2018 CX-9 vehicles because a wiring harness defect may disable the passenger air bag, turn signals, or engine starting system.
Proterra is recalling 2017-2018 Catalyst buses because defective swivel valves may fail to protect the air brake system from leaks, increasing crash risk.
Seats Incorporated is recalling ABTS 6-way seats because poor weld penetration may cause the seat to move unexpectedly, increasing injury risk in a crash.
Subaru is recalling 2019 Crosstrek vehicles because the driver's side rear-door window glass may be improperly tempered, posing an injury risk if it shatters.
Excel Industries is recalling about 5,400 zero-turn mowers because a wire tie could damage the fuel line, posing a fire hazard. No injuries have been reported.
Novartis is recalling Promacta (eltrombopag olamine) 12.5 mg oral suspension due to possible cross-contamination with peanut flour.
Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.
Integra LifeSciences is recalling MoniTorr CSF Drainage Systems due to a complaint trend regarding stopcock breakage.
Edwards Lifesciences is recalling EV1000 Clinical Platform monitors because liquid ingress into AC power outlets could cause an electrical short circuit and fire.
Integra LifeSciences is recalling LimiTorr and MoniTorr stopcock components due to a complaint trend regarding breakage.
Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.
Target is recalling approximately 90,000 heyday 3 Foot Lightning USB charging cables sold nationwide and online due to shock and fire hazards.
Beckman Coulter is recalling 2,059 UniCel DxH 600 hematology analyzers because they may produce erroneously elevated platelet results without warning, potentially masking low platelet counts.
Beckman Coulter is recalling UniCel DxH 800 analyzers because sporadic platelet results may be erroneously elevated without system flags, potentially leaving thrombocytopenia unrecognized.
Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 25 mg because FDA labs found an impurity above acceptable levels.