State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
MasterPharm LLC is recalling Finasteride Plus 1.25mg capsules nationwide because the product lacked processing controls to ensure it met specifications.
MasterPharm LLC is recalling 600 capsules of Progesterone Modified Release 100 mg due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Testosterone/Anastrozole Pellets 100/6 mg due to a lack of processing controls that ensures conformity to specifications.
Allergan is recalling 8,555 Skin Medica Acne System kits nationwide because the products failed potency tests at 12 and 24 months.
Indian Motorcycle is recalling 2019 Scout, Scout Sixty, and Scout Bobber models because trapped air in the brake system may reduce performance and increase crash risk.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because an open port on the fuel pump may leak fuel onto the roadway, increasing crash risk.
Triumph is recalling 2020 Tiger 900 motorcycles because rear reflectors may detach, reducing visibility and increasing crash risk.
Bentley is recalling 2020 Flying Spur vehicles because moisture can enter the rear camera holder, reducing image clarity and increasing crash risk.
USDA FSIS issued a public health alert for frozen taquitos and chimichangas that may contain hard plastic from recalled green chilies.
Hyundai is recalling 2020 Genesis G70 vehicles because a steering component may be defective, potentially causing the steering to lock or become difficult to operate while driving.
Mercedes-Benz is recalling specific 2017-2019 models because instrument cluster software may cause the seat belt warning system to display a solid light instead of a blinking light with an audible tone.
Certain 2018-2021 Autocar Xpeditor right-hand drive trucks may have improperly assembled parking brake plumbing, causing the brake to apply unexpectedly and increasing crash risk.
Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.
ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.
Bio Source Naturals is recalling Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a risk of poisoning to young children.
Miles Industries is recalling about 370 Valor H5 gas fireplaces in the U.S. because delayed ignition can shatter the glass window, posing burn and laceration risks.
General Motors is recalling 2020 Buick, Cadillac, Chevrolet, and GMC vehicles because the roof-rail air bag inflator may separate during deployment, increasing injury risk.
Xtreme Outdoors is recalling 2020 Little Guy Mini Max Trailers because understated weight ratings on certification labels may cause trailers to exceed tow vehicle capacity.
Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.
Winnebago is recalling 2019-2020 Micro Minnie 5 travel trailers because a bedroom emergency exit window was not installed, potentially preventing escape during an emergency.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to out-of-specification assay results in retention samples.
Boston Scientific is recalling 48 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Philips is recalling 28 IntelliVue MX800 patient monitors due to defective power supplies that may energize metal parts or prevent operation.
Carefusion 2200 Inc is recalling Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling IcePearl 2.0 CX 90 Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.